A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681029



Internal ID15070995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32409048..32409444hg38UCSC Ensembl
Innerchr9:32409046..32409442hg19UCSC Ensembl
Innerchr9:32399046..32399442hg18UCSC Ensembl
Innerchr9:32399046..32399442hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38397
hg19397
hg18397
hg17397
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521047
Supporting Variants
Samples
Known GenesACO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681029
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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