A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149223



Internal ID15855797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352069..57483628hg38UCSC Ensembl
Innerchr15:57644267..57775826hg19UCSC Ensembl
Innerchr15:55431559..55563118hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38131560
hg19131560
hg18131560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569585
Supporting Variants
Samples1782681495_A
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149223
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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