A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149583



Internal ID15531844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33742220..34134417hg38UCSC Ensembl
Innerchr15:34034421..34426618hg19UCSC Ensembl
Innerchr15:31821713..32213910hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38392198
hg19392198
hg18392198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568920
Supporting Variants
SamplesHGDP01215
Known GenesAVEN, CHRM5, EMC7, PGBD4, RYR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149583
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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