A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148659



Internal ID15877886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23403645..23530397hg38UCSC Ensembl
Innerchr15:23648792..23775544hg19UCSC Ensembl
Innerchr15:21200233..21326637hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38126753
hg19126753
hg18126405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568311
Supporting Variants
SamplesHGDP01063
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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