A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699166



Internal ID15089132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30040354..30053822hg38UCSC Ensembl
Innerchr9:30040352..30053820hg19UCSC Ensembl
Innerchr9:30030352..30043820hg18UCSC Ensembl
Innerchr9:30030352..30043820hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3813469
hg1913469
hg1813469
hg1713469
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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