A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674502



Internal ID15064468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30635284..30698144hg38UCSC Ensembl
Innerchr9:30635282..30698142hg19UCSC Ensembl
Innerchr9:30625282..30688142hg18UCSC Ensembl
Innerchr9:30625282..30688142hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3862861
hg1962861
hg1862861
hg1762861
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)nssv674502
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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