A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528683



Internal ID15109290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133488004..133488566hg38UCSC Ensembl
Innerchr8:134500247..134500809hg19UCSC Ensembl
Innerchr8:134569429..134569991hg18UCSC Ensembl
Innerchr8:134569429..134569991hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38563
hg19563
hg18563
hg17563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705325
Samples
Known GenesST3GAL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528683
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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