A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700202



Internal ID15436854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126167492..126185196hg38UCSC Ensembl
Innerchr9:128929771..128947475hg19UCSC Ensembl
Innerchr9:127969592..127987296hg18UCSC Ensembl
Innerchr9:126009325..126027029hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817705
hg1917705
hg1817705
hg1717705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524301
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700202
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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