A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518655



Internal ID15445948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18360149..18385958hg38UCSC Ensembl
Innerchr8:18217658..18243468hg19UCSC Ensembl
Innerchr8:18261938..18287748hg18UCSC Ensembl
Innerchr8:18261938..18287748hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3825810
hg1925811
hg1825811
hg1725811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696103
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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