A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567179



Internal ID16354588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20041701..21024079hg38UCSC Ensembl
Innerchr15:20246954..21229408hg19UCSC Ensembl
Innerchr15:18506968..19494067hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38982379
hg19982455
hg18987100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n54
Supporting Variantsnssv836917
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)nsv567179
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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