A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520423



Internal ID15447716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76432201..76450383hg38UCSC Ensembl
Innerchr9:79047117..79065299hg19UCSC Ensembl
Innerchr9:78236937..78255119hg18UCSC Ensembl
Innerchr9:76276671..76294853hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3818183
hg1918183
hg1818183
hg1718183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689821, nssv671339
Samples
Known GenesGCNT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520423
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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