A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145398



Internal ID15651898
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 StatusS
Merged Variantsnsv615608
Supporting Variants
Samples
Known GenesGBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145398
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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