A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622860



Internal ID7009718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33908123..33914481hg38UCSC Ensembl
Innerchr10:33908124..33914481hg38UCSC Ensembl
Outerchr10:33908123..33914482hg38UCSC Ensembl
chr10:34197051..34203409hg19UCSC Ensembl
Innerchr10:34197052..34203409hg19UCSC Ensembl
Outerchr10:34197051..34203410hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg386359
hg196359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13751443, essv13751432, essv13751428, essv13751446, essv13751433, essv13751437, essv13751420, essv13751425, essv13751424, essv13751439, essv13751426, essv13751434, essv13751429, essv13751438, essv13751445, essv13751421, essv13751441, essv13751448, essv13751430, essv13751436, essv13751422, essv13751440, essv13751427, essv13751431, essv13751447, essv13751450, essv13751449, essv13751442, essv13751435, essv13751423, essv13751444
SamplesNA19397, HG03247, HG02419, HG03130, NA19819, NA19377, HG02769, HG03385, NA19131, HG02315, HG02461, NA19471, HG02588, HG03352, HG03363, HG01880, HG01049, HG01102, NA19118, HG03451, HG02666, HG02772, NA19017, HG02557, HG03367, HG02721, HG02464, HG03432, HG03060, HG02643, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622860
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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