A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623950



Internal ID7010806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80228093..80234185hg38UCSC Ensembl
Innerchr10:80228093..80234185hg38UCSC Ensembl
Outerchr10:80227593..80234685hg38UCSC Ensembl
chr10:81987849..81993941hg19UCSC Ensembl
Innerchr10:81987849..81993941hg19UCSC Ensembl
Outerchr10:81987349..81994441hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386093
hg196093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870349, essv13870348, essv13870370, essv13870353, essv13870359, essv13870356, essv13870372, essv13870343, essv13870355, essv13870366, essv13870340, essv13870362, essv13870371, essv13870368, essv13870367, essv13870358, essv13870350, essv13870341, essv13870357, essv13870361, essv13870339, essv13870360, essv13870351, essv13870345, essv13870369, essv13870364, essv13870363, essv13870346, essv13870347, essv13870354, essv13870342, essv13870365, essv13870352, essv13870344
SamplesHG02614, HG03366, NA19703, HG02481, HG03247, HG01188, NA20332, HG03139, HG01140, HG03199, NA19374, HG03168, HG03105, HG02143, HG02315, NA19172, NA19471, NA18864, NA19908, NA19462, NA19236, HG03136, HG02283, HG03046, HG02330, NA19712, NA19324, NA19310, NA20281, NA19030, HG03162, NA19312, NA18511, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623950
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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