A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148661



Internal ID15877952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23437561..23530397hg38UCSC Ensembl
Innerchr15:23682708..23775544hg19UCSC Ensembl
Innerchr15:21234149..21326637hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3892837
hg1992837
hg1892489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568339
Supporting Variants
SamplesHGDP01072
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148661
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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