A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517832



Internal ID15445125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34791539..34815935hg38UCSC Ensembl
Innerchr9:34791536..34815932hg19UCSC Ensembl
Innerchr9:34781536..34805932hg18UCSC Ensembl
Innerchr9:34781536..34805932hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3824397
hg1924397
hg1824397
hg1724397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695236
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517832
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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