A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526378



Internal ID15453671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99282862..99293775hg38UCSC Ensembl
Innerchr9:102045144..102056057hg19UCSC Ensembl
Innerchr9:101084965..101095878hg18UCSC Ensembl
Innerchr9:99124699..99135612hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3810914
hg1910914
hg1810914
hg1710914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702674
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526378
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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