A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536036



Internal ID18834317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20283071..20833279hg38UCSC Ensembl
Innerchr15:20488324..21038608hg19UCSC Ensembl
Innerchr15:18748338..19303160hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38550209
hg19550285
hg18554823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048284
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)nssv3536036
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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