A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838124



Internal ID16132080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22087519..22094777hg38UCSC Ensembl
Innerchr15:22375470..22382728hg19UCSC Ensembl
Innerchr15:19876834..19884092hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387259
hg197259
hg187259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568046
Supporting Variants
Samples
Known GenesOR4N4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838124
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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