A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525298



Internal ID15452591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94527301..94550302hg38UCSC Ensembl
Innerchr9:97289583..97312584hg19UCSC Ensembl
Innerchr9:96329404..96352405hg18UCSC Ensembl
Innerchr9:94369138..94392139hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3823002
hg1923002
hg1823002
hg1723002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701404
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525298
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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