A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981354



Internal ID12626540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726505..32152007hg38UCSC Ensembl
Innerchr15:32018708..32444208hg19UCSC Ensembl
Innerchr15:29806000..30231500hg18UCSC Ensembl
Innerchr15:29806000..30231500hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38425503
hg19425501
hg18425501
hg17425501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751531
Supporting Variants
SamplesBEC_394
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981354
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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