A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3534494



Internal ID18832775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20376299hg38UCSC Ensembl
Innerchr15:20203949..20581552hg19UCSC Ensembl
Innerchr15:18463963..18841566hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38377604
hg19377604
hg18377604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038908
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)nssv3534494
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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