A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519883



Internal ID15447176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15757441..15836461hg38UCSC Ensembl
Innerchr20:15738086..15817106hg19UCSC Ensembl
Innerchr20:15686086..15765106hg18UCSC Ensembl
Innerchr20:15686086..15765106hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3879021
hg1979021
hg1879021
hg1779021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694352
Samples
Known GenesMACROD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519883
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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