A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3534822



Internal ID18833103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20248994..20796091hg38UCSC Ensembl
Innerchr15:20454247..21001420hg19UCSC Ensembl
Innerchr15:18714261..19261474hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38547098
hg19547174
hg18547214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051608
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3534822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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