A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521193



Internal ID15448486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20331683..20337133hg38UCSC Ensembl
Innerchr9:20331681..20337131hg19UCSC Ensembl
Innerchr9:20321681..20327131hg18UCSC Ensembl
Innerchr9:20321681..20327131hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385451
hg195451
hg185451
hg175451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686213, nssv684291, nssv689693
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521193
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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