A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614091



Internal ID7000986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89890547..89901207hg38UCSC Ensembl
Innerchr7:89890547..89901207hg38UCSC Ensembl
Outerchr7:89890274..89901509hg38UCSC Ensembl
chr7:89519861..89530521hg19UCSC Ensembl
Innerchr7:89519861..89530521hg19UCSC Ensembl
Outerchr7:89519588..89530823hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3810661
hg1910661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12882342, essv12882236, essv12882218, essv12882324, essv12882310, essv12882346, essv12882243, essv12882227, essv12882267, essv12882341, essv12882316, essv12882326, essv12882291, essv12882214, essv12882313, essv12882289, essv12882265, essv12882319, essv12882263, essv12882229, essv12882290, essv12882235, essv12882306, essv12882331, essv12882293, essv12882261, essv12882308, essv12882287, essv12882256, essv12882219, essv12882336, essv12882284, essv12882335, essv12882295, essv12882264, essv12882269, essv12882238, essv12882288, essv12882322, essv12882225, essv12882270, essv12882228, essv12882302, essv12882221, essv12882217, essv12882241, essv12882294, essv12882273, essv12882307, essv12882329, essv12882215, essv12882328, essv12882314, essv12882344, essv12882333, essv12882296, essv12882260, essv12882285, essv12882300, essv12882268, essv12882315, essv12882274, essv12882250, essv12882332, essv12882320, essv12882286, essv12882216, essv12882231, essv12882345, essv12882257, essv12882338, essv12882334, essv12882280, essv12882224, essv12882275, essv12882347, essv12882247, essv12882292, essv12882271, essv12882279, essv12882232, essv12882220, essv12882321, essv12882305, essv12882255, essv12882248, essv12882327, essv12882337, essv12882301, essv12882252, essv12882246, essv12882258, essv12882222, essv12882330, essv12882297, essv12882233, essv12882340, essv12882325, essv12882317, essv12882234, essv12882254, essv12882278, essv12882239, essv12882318, essv12882304, essv12882213, essv12882237, essv12882283, essv12882282, essv12882272, essv12882343, essv12882276, essv12882251, essv12882249, essv12882309, essv12882311, essv12882230, essv12882298, essv12882299, essv12882262, essv12882259, essv12882242, essv12882244, essv12882339, essv12882277, essv12882266, essv12882281, essv12882323, essv12882245, essv12882240, essv12882223, essv12882303, essv12882226, essv12882253, essv12882312
SamplesNA18745, HG00235, HG00121, HG03652, HG01965, HG01303, HG00102, NA18947, HG00351, NA20899, HG02433, NA12843, NA11933, HG00233, HG00452, NA19777, NA19684, HG01971, HG03895, HG01518, HG00261, HG00097, HG03950, NA12341, HG01341, HG01506, HG01325, HG01070, NA20798, NA19764, HG03808, NA19771, HG01528, HG00355, HG01510, HG03762, HG00139, HG02493, HG01069, HG03910, HG01398, HG01067, NA20518, HG01519, HG01072, HG01767, HG01673, NA12815, HG01440, HG01048, NA12828, HG00178, HG00253, NA19789, NA20755, NA20753, NA10847, HG00137, NA20904, HG00268, NA19707, HG02233, HG03787, HG03644, NA21119, HG00190, HG02397, HG01095, HG00701, HG04195, HG01515, HG00101, NA20536, HG02253, HG02322, HG03771, HG00275, NA20767, NA18534, HG00551, HG00619, HG01092, HG01447, HG03742, HG01615, HG04054, HG02604, HG01130, HG00321, HG03854, HG03745, HG00704, HG00141, HG04159, NA12778, NA12546, HG01589, HG03743, HG00407, NA20872, NA12716, HG04216, HG01678, NA19072, HG04186, HG00375, HG01362, NA20804, HG01623, NA20792, HG01205, NA20902, NA19439, HG01620, NA12763, HG04003, HG01395, HG00111, NA20582, NA21102, HG01783, HG00112, NA19080, HG01468, HG03611, HG01125, HG01566, HG00759, NA12154, HG04061, HG01786, NA20754, HG01437, HG00978, NA11832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614091
Frequency
Sample Size2504
Observed Gain0
Observed Loss135
Observed Complex0
Frequencyn/a


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