A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518696



Internal ID15099303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86320473..86337398hg38UCSC Ensembl
Innerchr9:88935388..88952313hg19UCSC Ensembl
Innerchr9:88125208..88142133hg18UCSC Ensembl
Innerchr9:86164942..86181867hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3816926
hg1916926
hg1816926
hg1716926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696147
Samples
Known GenesZCCHC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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