A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528721



Internal ID15456014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38838478..38852035hg38UCSC Ensembl
Innerchr8:38695996..38709553hg19UCSC Ensembl
Innerchr8:38815153..38828710hg18UCSC Ensembl
Innerchr8:38815153..38828710hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3813558
hg1913558
hg1813558
hg1713558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705375
Samples
Known GenesTACC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528721
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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