A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839662



Internal ID16133618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726528..32151722hg38UCSC Ensembl
Innerchr15:32018731..32443923hg19UCSC Ensembl
Innerchr15:29806023..30231215hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38425195
hg19425193
hg18425193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568830
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839662
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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