A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149243



Internal ID15533089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78615690..78727268hg38UCSC Ensembl
Innerchr15:78908032..79019610hg19UCSC Ensembl
Innerchr15:76695087..76806665hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38111579
hg19111579
hg18111579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570201
Supporting Variants
SamplesNINDS_105
Known GenesCHRNA3, CHRNB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149243
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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