A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518953



Internal ID15446246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54662091..54671963hg38UCSC Ensembl
Innerchr19:55173542..55183414hg19UCSC Ensembl
Innerchr19:59865354..59875226hg18UCSC Ensembl
Innerchr19:59865354..59875226hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg389873
hg199873
hg189873
hg179873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696421
Samples
Known GenesLILRB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518953
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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