A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716716



Internal ID19014997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43721941hg38UCSC Ensembl
Innerchr15:43893072..44014139hg19UCSC Ensembl
Innerchr15:41680364..41801431hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38121068
hg19121068
hg18121068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054620
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1A, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716716
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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