A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615608



Internal ID16056331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133092699..133162355hg38UCSC Ensembl
Innerchr9:135968086..136037742hg19UCSC Ensembl
Innerchr9:134957907..135027563hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3869657
hg1969657
hg1869657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12928n54
Supporting Variantsnssv1145398
Samples
Known GenesGBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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