A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843564



Internal ID16137520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352258..57470595hg38UCSC Ensembl
Innerchr15:57644456..57762793hg19UCSC Ensembl
Innerchr15:55431748..55550085hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38118338
hg19118338
hg18118338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569586
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)nssv843564
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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