A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34498



Internal ID12990535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1810597..1881202hg38UCSC Ensembl
Innerchr10:1852791..1923396hg19UCSC Ensembl
Innerchr10:1842791..1913396hg18UCSC Ensembl
Innerchr10:1842791..1913396hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3870606
hg1970606
hg1870606
hg1770606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18e55
Supporting Variantsessv6978175, essv6978174, essv6990205, essv6978173
SamplesNA18974
Known Genes
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)esv34498
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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