A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567201



Internal ID16354610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20054126..21024079hg38UCSC Ensembl
Innerchr15:20259379..21229408hg19UCSC Ensembl
Innerchr15:18519393..19494067hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38969954
hg19970030
hg18974675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4164n54
Supporting Variantsnssv836950
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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