A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622450



Internal ID6662620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15627778..15632265hg38UCSC Ensembl
Innerchr10:15627778..15632265hg38UCSC Ensembl
Outerchr10:15627546..15632564hg38UCSC Ensembl
chr10:15669777..15674264hg19UCSC Ensembl
Innerchr10:15669777..15674264hg19UCSC Ensembl
Outerchr10:15669545..15674563hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384488
hg194488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704472, essv13704460, essv13704473, essv13704469, essv13704471, essv13704456, essv13704465, essv13704461, essv13704464, essv13704470, essv13704458, essv13704459, essv13704466, essv13704453, essv13704468, essv13704457, essv13704454, essv13704462, essv13704467, essv13704463, essv13704455, essv13704452, essv13704451
SamplesHG02614, HG03366, HG02589, HG03135, HG03452, HG03578, NA19457, HG02981, HG02573, HG02588, NA18520, HG02968, HG02537, HG03311, HG02568, HG02675, HG03028, HG03240, HG03433, HG02814, NA19117, HG03066, NA18522
Known GenesITGA8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622450
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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