A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518603



Internal ID15445896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130095207..130097609hg38UCSC Ensembl
Innerchr9:132857486..132859888hg19UCSC Ensembl
Innerchr9:131897307..131899709hg18UCSC Ensembl
Innerchr9:129937040..129939442hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382403
hg192403
hg182403
hg172403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696049
Samples
Known GenesGPR107
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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