A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149597



Internal ID15875829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47814724..48058126hg38UCSC Ensembl
Innerchr15:48106921..48350323hg19UCSC Ensembl
Innerchr15:45894213..46137615hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38243403
hg19243403
hg18243403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569335
Supporting Variants
SamplesHGDP00741
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149597
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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