A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843567



Internal ID16137523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352258..57498238hg38UCSC Ensembl
Innerchr15:57644456..57790436hg19UCSC Ensembl
Innerchr15:55431748..55577728hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38145981
hg19145981
hg18145981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569588
Supporting Variants
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843567
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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