A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611289



Internal ID6998198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152905407..152906605hg38UCSC Ensembl
Innerchr6:152905407..152906605hg38UCSC Ensembl
Outerchr6:152905318..152906760hg38UCSC Ensembl
chr6:153226542..153227740hg19UCSC Ensembl
Innerchr6:153226542..153227740hg19UCSC Ensembl
Outerchr6:153226453..153227895hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12586231, essv12586292, essv12586240, essv12586280, essv12586249, essv12586268, essv12586232, essv12586271, essv12586244, essv12586239, essv12586261, essv12586283, essv12586266, essv12586242, essv12586236, essv12586241, essv12586274, essv12586228, essv12586262, essv12586224, essv12586267, essv12586284, essv12586257, essv12586237, essv12586227, essv12586263, essv12586264, essv12586256, essv12586265, essv12586270, essv12586247, essv12586289, essv12586282, essv12586234, essv12586286, essv12586275, essv12586226, essv12586291, essv12586281, essv12586225, essv12586278, essv12586276, essv12586285, essv12586273, essv12586251, essv12586277, essv12586245, essv12586230, essv12586288, essv12586279, essv12586250, essv12586259, essv12586269, essv12586229, essv12586272, essv12586290, essv12586248, essv12586246, essv12586255, essv12586233, essv12586287, essv12586253, essv12586235, essv12586243, essv12586238, essv12586258, essv12586260, essv12586254, essv12586293, essv12586294, essv12586252
SamplesHG01985, HG02628, HG03548, NA18508, HG03163, HG02318, HG03115, HG03298, HG02589, NA19443, HG03074, NA19448, HG03091, NA20317, HG02562, HG02143, HG02561, HG03212, HG02461, HG02885, NA19036, NA19026, HG02571, HG03267, NA20318, HG02479, HG03120, HG02570, HG03061, NA19462, HG03547, HG02511, NA19043, NA19236, HG03123, HG03085, NA19114, HG02429, HG03136, NA18499, NA18853, HG03024, HG02594, HG01956, HG01148, NA19440, HG02667, NA19147, HG02799, NA19434, NA19454, HG01894, HG03117, NA19331, HG02923, HG02837, HG01174, NA19334, HG02839, HG02317, HG03557, NA19328, HG03432, HG02646, NA19468, NA19474, HG02107, HG03351, HG03410, HG03376, HG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611289
Frequency
Sample Size2504
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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