A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518857



Internal ID15446150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69339795..69342195hg38UCSC Ensembl
Innerchr8:70252030..70254430hg19UCSC Ensembl
Innerchr8:70414584..70416984hg18UCSC Ensembl
Innerchr8:70414584..70416984hg17UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382401
hg192401
hg182401
hg172401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696311
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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