A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527877



Internal ID15455170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121413842..121460057hg38UCSC Ensembl
Innerchr8:122426082..122472297hg19UCSC Ensembl
Innerchr8:122495263..122541478hg18UCSC Ensembl
Innerchr8:122495263..122541478hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3846216
hg1946216
hg1846216
hg1746216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704378
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527877
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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