A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522609



Internal ID15449902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126029224..126030700hg38UCSC Ensembl
Innerchr9:128791503..128792979hg19UCSC Ensembl
Innerchr9:127831324..127832800hg18UCSC Ensembl
Innerchr9:125871057..125872533hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381477
hg191477
hg181477
hg171477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706001
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522609
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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