A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537918



Internal ID18836199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..20806746hg38UCSC Ensembl
Innerchr15:20291301..21012075hg19UCSC Ensembl
Innerchr15:18551315..19272115hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38720699
hg19720775
hg18720801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052164
Supporting Variants
Samples
Known GenesCHEK2P2, CXADRP2, 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)nssv3537918
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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