A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567402



Internal ID16354811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20377603..20610560hg38UCSC Ensembl
Innerchr15:20582856..20815866hg19UCSC Ensembl
Innerchr15:18842870..19075880hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38232958
hg19233011
hg18233011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4203n54
Supporting Variantsnssv837223
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567402
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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