A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520662



Internal ID15447955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133669313..133673822hg38UCSC Ensembl
Innerchr8:134681556..134686065hg19UCSC Ensembl
Innerchr8:134750738..134755247hg18UCSC Ensembl
Innerchr8:134750738..134755247hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384510
hg194510
hg184510
hg174510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697543
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520662
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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