A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518896



Internal ID15446189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:50838374..50877333hg38UCSC Ensembl
Innerchr20:49454911..49493870hg19UCSC Ensembl
Innerchr20:48888318..48927277hg18UCSC Ensembl
Innerchr20:48888318..48927277hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3838960
hg1938960
hg1838960
hg1738960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696355
Samples
Known GenesBCAS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518896
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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