A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990489



Internal ID12982516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44831410..44976010hg38UCSC Ensembl
Innerchr15:45123608..45268208hg19UCSC Ensembl
Innerchr15:42910900..43055500hg18UCSC Ensembl
Innerchr15:42910900..43055500hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144601
hg19144601
hg18144601
hg17144601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34494
Supporting Variants
SamplesNA19202
Known GenesC15orf43
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990489
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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