A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838129



Internal ID16132085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22087787..22094185hg38UCSC Ensembl
Innerchr15:22375738..22382136hg19UCSC Ensembl
Innerchr15:19877102..19883500hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386399
hg196399
hg186399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568051
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838129
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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