A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524217



Internal ID15451510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133030314..133030670hg38UCSC Ensembl
Innerchr9:135905701..135906057hg19UCSC Ensembl
Innerchr9:134895522..134895878hg18UCSC Ensembl
Innerchr9:132935255..132935611hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38357
hg19357
hg18357
hg17357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700105
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524217
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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