A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978917



Internal ID12632649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22032106..22300068hg38UCSC Ensembl
Innerchr15:22320057..22588019hg19UCSC Ensembl
Innerchr15:19821421..20089383hg18UCSC Ensembl
Innerchr15:19821421..20089383hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38267963
hg19267963
hg18267963
hg17267963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35054
Supporting Variants
SamplesNA12762
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978917
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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