A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519470



Internal ID15446763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:204470907..204472677hg38UCSC Ensembl
Innerchr2:205335630..205337400hg19UCSC Ensembl
Innerchr2:205043875..205045645hg18UCSC Ensembl
Innerchr2:205161136..205162906hg17UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381771
hg191771
hg181771
hg171771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696870
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519470
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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