A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516678



Internal ID15443971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46802826..46805760hg38UCSC Ensembl
Innerchr20:45431465..45434399hg19UCSC Ensembl
Innerchr20:44864872..44867806hg18UCSC Ensembl
Innerchr20:44864872..44867806hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382935
hg192935
hg182935
hg172935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662277, nssv670100
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516678
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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