A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519420



Internal ID15446713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133290774..133299471hg38UCSC Ensembl
Innerchr9:136166346..136175051hg19UCSC Ensembl
Innerchr9:135156167..135164872hg18UCSC Ensembl
Innerchr9:133195900..133204605hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388698
hg198706
hg188706
hg178706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696844
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519420
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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