A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667485



Internal ID15404137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11905556..11965111hg38UCSC Ensembl
Innerchr9:11905556..11965111hg19UCSC Ensembl
Innerchr9:11895556..11955111hg18UCSC Ensembl
Innerchr9:11895556..11955111hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3859556
hg1959556
hg1859556
hg1759556
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667485
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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