A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567350



Internal ID16354759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20367552..21097326hg38UCSC Ensembl
Innerchr15:20572805..21302655hg19UCSC Ensembl
Innerchr15:18832819..19567314hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38729775
hg19729851
hg18734496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4182n54
Supporting Variantsnssv837147
Samples
Known GenesCT60, 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)nsv567350
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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