A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517032



Internal ID15444325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16580345..16604669hg38UCSC Ensembl
Innerchr20:16560990..16585314hg19UCSC Ensembl
Innerchr20:16508990..16533314hg18UCSC Ensembl
Innerchr20:16508990..16533314hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3824325
hg1924325
hg1824325
hg1724325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661327, nssv682295, nssv664734, nssv657279, nssv662021, nssv665632, nssv670612, nssv690867, nssv676486, nssv685963, nssv670481, nssv665873, nssv688771, nssv674685, nssv659300, nssv685818, nssv693909, nssv653647, nssv680713
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517032
Frequency
Sample Size2026
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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