A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526891



Internal ID15454184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126224800..126225555hg38UCSC Ensembl
Innerchr9:128987079..128987834hg19UCSC Ensembl
Innerchr9:128026900..128027655hg18UCSC Ensembl
Innerchr9:126066633..126067388hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38756
hg19756
hg18756
hg17756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703249
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526891
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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