A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700296



Internal ID15090262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15165034..15202419hg38UCSC Ensembl
Innerchr9:15165032..15202417hg19UCSC Ensembl
Innerchr9:15155032..15192417hg18UCSC Ensembl
Innerchr9:15155032..15192417hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3837386
hg1937386
hg1837386
hg1737386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524381
Supporting Variants
Samples
Known GenesTTC39B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700296
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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