A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526686



Internal ID15453979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129796727..129826886hg38UCSC Ensembl
Innerchr8:130808973..130839132hg19UCSC Ensembl
Innerchr8:130878155..130908314hg18UCSC Ensembl
Innerchr8:130878155..130908314hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3830160
hg1930160
hg1830160
hg1730160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703019
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526686
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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