A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518522



Internal ID15445815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105664454..105664503hg38UCSC Ensembl
Innerchr9:108426735..108426784hg19UCSC Ensembl
Innerchr9:107466556..107466605hg18UCSC Ensembl
Innerchr9:105506290..105506339hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
hg1750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695963
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518522
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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