A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705375



Internal ID15442027
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528721
Supporting Variants
Samples
Known GenesTACC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705375
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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