A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567466



Internal ID16354875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20419601..20627136hg38UCSC Ensembl
Innerchr15:20624854..20832439hg19UCSC Ensembl
Innerchr15:18884868..19092453hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38207536
hg19207586
hg18207586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4203n54
Supporting Variantsnssv837299
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)nsv567466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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