A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525416



Internal ID15452709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121413096..121433082hg38UCSC Ensembl
Innerchr8:122425336..122445322hg19UCSC Ensembl
Innerchr8:122494517..122514503hg18UCSC Ensembl
Innerchr8:122494517..122514503hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3819987
hg1919987
hg1819987
hg1719987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701540
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525416
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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