A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713683



Internal ID19011964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20267586..20926480hg38UCSC Ensembl
Innerchr15:20472839..21131809hg19UCSC Ensembl
Innerchr15:18732853..19396468hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38658895
hg19658971
hg18663616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039704
Supporting Variants
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713683
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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