A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621829



Internal ID7008695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129302787..129305145hg38UCSC Ensembl
Innerchr9:129302788..129305145hg38UCSC Ensembl
Outerchr9:129302787..129305146hg38UCSC Ensembl
chr9:132065066..132067424hg19UCSC Ensembl
Innerchr9:132065067..132067424hg19UCSC Ensembl
Outerchr9:132065066..132067425hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628256, essv13628182, essv13628171, essv13628161, essv13628299, essv13628268, essv13628227, essv13628118, essv13628291, essv13628228, essv13628219, essv13628139, essv13628303, essv13628290, essv13628140, essv13628273, essv13628196, essv13628153, essv13628295, essv13628246, essv13628244, essv13628213, essv13628292, essv13628214, essv13628270, essv13628195, essv13628183, essv13628156, essv13628261, essv13628159, essv13628122, essv13628184, essv13628143, essv13628190, essv13628162, essv13628165, essv13628238, essv13628135, essv13628120, essv13628125, essv13628147, essv13628279, essv13628288, essv13628278, essv13628230, essv13628258, essv13628129, essv13628298, essv13628217, essv13628177, essv13628158, essv13628181, essv13628272, essv13628160, essv13628239, essv13628192, essv13628186, essv13628119, essv13628265, essv13628146, essv13628231, essv13628255, essv13628218, essv13628166, essv13628286, essv13628203, essv13628142, essv13628259, essv13628296, essv13628267, essv13628274, essv13628250, essv13628204, essv13628130, essv13628202, essv13628151, essv13628210, essv13628245, essv13628251, essv13628145, essv13628123, essv13628281, essv13628138, essv13628264, essv13628226, essv13628172, essv13628266, essv13628211, essv13628191, essv13628193, essv13628280, essv13628241, essv13628225, essv13628236, essv13628117, essv13628252, essv13628215, essv13628237, essv13628285, essv13628164, essv13628127, essv13628194, essv13628233, essv13628169, essv13628301, essv13628275, essv13628136, essv13628287, essv13628220, essv13628198, essv13628132, essv13628154, essv13628150, essv13628283, essv13628141, essv13628180, essv13628247, essv13628229, essv13628224, essv13628297, essv13628222, essv13628175, essv13628179, essv13628304, essv13628170, essv13628263, essv13628155, essv13628200, essv13628257, essv13628137, essv13628212, essv13628174, essv13628294, essv13628116, essv13628216, essv13628234, essv13628207, essv13628249, essv13628185, essv13628243, essv13628205, essv13628282, essv13628289, essv13628248, essv13628121, essv13628284, essv13628134, essv13628277, essv13628206, essv13628189, essv13628133, essv13628260, essv13628223, essv13628276, essv13628167, essv13628168, essv13628157, essv13628262, essv13628235, essv13628187, essv13628176, essv13628197, essv13628148, essv13628131, essv13628201, essv13628221, essv13628128, essv13628271, essv13628126, essv13628302, essv13628300, essv13628253, essv13628144, essv13628124, essv13628269, essv13628173, essv13628242, essv13628152, essv13628232, essv13628208, essv13628240, essv13628163, essv13628188, essv13628178, essv13628209, essv13628254, essv13628199, essv13628149, essv13628293
SamplesNA21091, HG04198, HG02386, NA20882, HG03773, HG00542, HG00592, NA21097, HG01795, NA19794, HG02272, HG01462, NA21089, HG02002, HG00524, HG02375, NA20899, HG03753, NA18561, HG01326, HG02661, HG02727, HG02275, NA18641, NA19795, HG04094, HG02277, HG01486, NA19057, NA19684, HG03667, HG02271, HG01947, HG00449, HG02734, HG03950, NA20894, HG01250, NA19792, NA19746, HG04100, HG01341, NA21135, HG03016, HG03706, HG03640, NA18595, HG02491, HG01997, NA20911, HG01968, HG03913, NA18618, HG03905, HG03885, HG04070, NA21103, NA19782, HG02786, HG01859, HG03851, HG03619, HG04214, HG02067, HG03595, NA19731, HG03746, HG02082, HG01405, NA21107, NA20869, HG01932, HG04185, NA21129, HG02104, NA18557, HG01121, HG03585, HG00419, NA21122, NA18648, HG00743, HG01942, HG01565, HG01124, NA18645, NA18614, HG02402, HG03844, NA18605, NA18613, NA19657, HG02136, HG01435, NA20858, HG02793, HG03787, HG02345, HG02090, NA21119, HG01271, HG00653, HG03928, HG01938, NA19663, HG02731, HG03900, HG03771, HG00500, HG03775, HG03805, NA18572, HG01323, HG03967, NA18573, HG03871, NA18626, HG00404, HG03951, HG03858, HG03713, HG02604, HG02048, HG02008, HG02657, NA20856, HG04189, HG03953, HG03745, HG02724, HG02081, HG03969, NA18555, HG03914, HG02031, HG04118, NA18593, NA18945, HG01811, NA18953, HG03720, NA19729, NA18542, HG02684, HG04188, NA18543, HG04006, HG01131, HG04239, HG02696, HG02682, NA19732, NA20870, HG02304, NA20351, NA21123, HG03702, HG03869, NA21095, HG03727, NA21126, NA19783, HG02019, HG03019, NA20887, NA20888, NA19759, HG03600, HG01432, HG04015, NA21088, HG02147, HG03977, HG04014, NA21133, HG03684, HG03615, NA19770, HG02681, NA19661, HG01431, HG00472, NA19004, NA19758, HG02778, NA18623, HG03931, HG03815, HG01923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621829
Frequency
Sample Size2504
Observed Gain0
Observed Loss189
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer