A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518442



Internal ID15099049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56414270..56429946hg38UCSC Ensembl
Innerchr20:54989326..55005002hg19UCSC Ensembl
Innerchr20:54422733..54438409hg18UCSC Ensembl
Innerchr20:54422733..54438409hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815677
hg1915677
hg1815677
hg1715677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694237
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518442
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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