A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696139



Internal ID15432791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51842991..51844792hg38UCSC Ensembl
Innerchr20:50459530..50461331hg19UCSC Ensembl
Innerchr20:49892937..49894738hg18UCSC Ensembl
Innerchr20:49892937..49894738hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381802
hg191802
hg181802
hg171802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518686
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696139
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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