A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521120



Internal ID15101727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128803275..128829871hg38UCSC Ensembl
Innerchr9:131565554..131592150hg19UCSC Ensembl
Innerchr9:130605375..130631971hg18UCSC Ensembl
Innerchr9:128645108..128671704hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3826597
hg1926597
hg1826597
hg1726597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687845, nssv682564
Samples
Known GenesC9orf114, ENDOG, TBC1D13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521120
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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