A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696410



Internal ID15433062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20960171..20988667hg38UCSC Ensembl
Innerchr9:20960170..20988666hg19UCSC Ensembl
Innerchr9:20950170..20978666hg18UCSC Ensembl
Innerchr9:20950170..20978666hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828497
hg1928497
hg1828497
hg1728497
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518943
Supporting Variants
Samples
Known GenesFOCAD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696410
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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