A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980371



Internal ID12631588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22032106..22216247hg38UCSC Ensembl
Innerchr15:22320057..22504198hg19UCSC Ensembl
Innerchr15:19821421..20005562hg18UCSC Ensembl
Innerchr15:19821421..20005562hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38184142
hg19184142
hg18184142
hg17184142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34696
Supporting Variants
SamplesNA07357
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980371
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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