A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631823



Internal ID7018632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38804910..38809291hg38UCSC Ensembl
Innerchr13:38804910..38809291hg38UCSC Ensembl
Outerchr13:38804784..38809619hg38UCSC Ensembl
chr13:39379047..39383428hg19UCSC Ensembl
Innerchr13:39379047..39383428hg19UCSC Ensembl
Outerchr13:39378921..39383756hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384382
hg194382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14699370, essv14699274, essv14699361, essv14699340, essv14699289, essv14699276, essv14699304, essv14699353, essv14699343, essv14699300, essv14699308, essv14699360, essv14699298, essv14699358, essv14699296, essv14699356, essv14699366, essv14699305, essv14699322, essv14699364, essv14699278, essv14699369, essv14699315, essv14699299, essv14699310, essv14699334, essv14699367, essv14699286, essv14699280, essv14699302, essv14699284, essv14699271, essv14699290, essv14699319, essv14699318, essv14699273, essv14699337, essv14699288, essv14699362, essv14699303, essv14699277, essv14699365, essv14699325, essv14699312, essv14699297, essv14699272, essv14699327, essv14699294, essv14699306, essv14699266, essv14699267, essv14699354, essv14699341, essv14699355, essv14699359, essv14699295, essv14699335, essv14699283, essv14699350, essv14699269, essv14699348, essv14699330, essv14699311, essv14699338, essv14699331, essv14699342, essv14699265, essv14699332, essv14699313, essv14699291, essv14699363, essv14699307, essv14699323, essv14699352, essv14699317, essv14699320, essv14699275, essv14699316, essv14699287, essv14699371, essv14699279, essv14699346, essv14699282, essv14699351, essv14699336, essv14699268, essv14699264, essv14699281, essv14699309, essv14699285, essv14699328, essv14699324, essv14699357, essv14699292, essv14699301, essv14699349, essv14699326, essv14699329, essv14699321, essv14699333, essv14699314, essv14699339, essv14699368, essv14699270, essv14699344, essv14699347, essv14699345, essv14699293
SamplesHG00536, NA19914, HG01860, HG04194, NA18599, HG00457, NA18528, NA19350, NA18639, HG00699, NA19057, HG02382, NA18959, HG02040, NA18962, HG03796, HG01853, NA18635, NA18993, HG01843, NA18571, HG04183, NA18977, HG01813, HG02187, NA19372, HG00534, NA19075, NA18966, NA19087, HG00406, NA18640, NA18973, HG00543, NA18951, HG02136, HG01841, NA19070, NA19056, NA18525, HG02070, HG02142, HG02025, HG01857, NA19077, HG02697, HG00428, HG00701, HG04162, HG03491, HG01810, HG01845, HG00598, HG00583, NA19081, HG00500, HG02522, NA18572, NA18976, HG01796, HG00692, NA18548, HG02364, NA18573, HG03858, NA19001, HG02086, HG00613, NA19761, HG00704, NA18570, HG00410, HG02127, HG00445, NA18646, NA19003, HG01858, HG01812, HG03833, NA18952, HG00625, NA19454, NA19072, HG01800, HG02391, NA19334, HG01866, HG01598, NA19786, NA18591, NA19083, HG02139, NA19360, HG02137, NA18615, HG01801, HG03600, HG02128, HG00513, HG02373, HG02367, HG01868, NA18636, NA20886, HG00472, NA19312, HG00628, NA18612
Known GenesFREM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631823
Frequency
Sample Size2504
Observed Gain0
Observed Loss108
Observed Complex0
Frequencyn/a


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