A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838659



Internal ID16132615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24214032..24496144hg38UCSC Ensembl
Innerchr15:24459179..24741291hg19UCSC Ensembl
Innerchr15:22010272..22292384hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38282113
hg19282113
hg18282113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568464
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)nssv838659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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