A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34804



Internal ID12990840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1810597..1875160hg38UCSC Ensembl
Innerchr10:1852791..1917354hg19UCSC Ensembl
Innerchr10:1842791..1907354hg18UCSC Ensembl
Innerchr10:1842791..1907354hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864564
hg1964564
hg1864564
hg1764564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18e55
Supporting Variantsessv6990443, essv6980095, essv6980096
SamplesNA18952
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34804
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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