A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715703



Internal ID19013984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20373156hg38UCSC Ensembl
Innerchr15:20203949..20578409hg19UCSC Ensembl
Innerchr15:18463963..18838423hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38374461
hg19374461
hg18374461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044359
Supporting Variants
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715703
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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