A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517931



Internal ID15445224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59053184..59085809hg38UCSC Ensembl
Innerchr20:57628239..57660864hg19UCSC Ensembl
Innerchr20:57061634..57094259hg18UCSC Ensembl
Innerchr20:57061634..57094259hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3832626
hg1932626
hg1832626
hg1732626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695343
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517931
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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