A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34494



Internal ID12990531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44813678..44976010hg38UCSC Ensembl
Innerchr15:45105876..45268208hg19UCSC Ensembl
Innerchr15:42893168..43055500hg18UCSC Ensembl
Innerchr15:42893168..43055500hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38162333
hg19162333
hg18162333
hg17162333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6990489, essv6986004, essv6980493
SamplesNA19202
Known GenesC15orf43
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)esv34494
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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