A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34623



Internal ID12990659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623811..5674895hg38UCSC Ensembl
Innerchr10:5665774..5716858hg19UCSC Ensembl
Innerchr10:5705780..5756864hg18UCSC Ensembl
Innerchr10:5705780..5756864hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851085
hg1951085
hg1851085
hg1751085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv19e55
Supporting Variantsessv6985430, essv6980907
SamplesNA19143
Known GenesASB13
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34623
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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