A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538216



Internal ID18836497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20210878..20929146hg38UCSC Ensembl
Innerchr15:20416131..21134475hg19UCSC Ensembl
Innerchr15:18676145..19399134hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38718269
hg19718345
hg18722990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049109
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)nssv3538216
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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