A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569099



Internal ID16009822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450532..34545691hg38UCSC Ensembl
Innerchr15:34742733..34837892hg19UCSC Ensembl
Innerchr15:32530025..32625184hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3895160
hg1995160
hg1895160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4476n54
Supporting Variantsnssv840337
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569099
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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