A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3717937



Internal ID19016218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57340817..57494222hg38UCSC Ensembl
Innerchr15:57633015..57786420hg19UCSC Ensembl
Innerchr15:55420307..55573712hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38153406
hg19153406
hg18153406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038663
Supporting Variants
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3717937
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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