A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843563



Internal ID16137519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352069..57483608hg38UCSC Ensembl
Innerchr15:57644267..57775806hg19UCSC Ensembl
Innerchr15:55431559..55563098hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38131540
hg19131540
hg18131540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569584
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)nssv843563
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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