A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519447



Internal ID15100054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32456658..32457560hg38UCSC Ensembl
Innerchr9:32456656..32457558hg19UCSC Ensembl
Innerchr9:32446656..32447558hg18UCSC Ensembl
Innerchr9:32446656..32447558hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38903
hg19903
hg18903
hg17903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693754, nssv656223
Samples
Known GenesDDX58
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519447
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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