A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518928



Internal ID15446221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:204219716..204225922hg38UCSC Ensembl
Innerchr2:205084439..205090645hg19UCSC Ensembl
Innerchr2:204792684..204798890hg18UCSC Ensembl
Innerchr2:204909945..204916151hg17UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg386207
hg196207
hg186207
hg176207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696394
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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