A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568936



Internal ID16009659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34402116..34552372hg38UCSC Ensembl
Innerchr15:34694317..34844573hg19UCSC Ensembl
Innerchr15:32481609..32631865hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38150257
hg19150257
hg18150257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4459n54
Supporting Variantsnssv839813
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568936
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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