A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528024



Internal ID15455317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12321800..12365588hg38UCSC Ensembl
Innerchr20:12302448..12346236hg19UCSC Ensembl
Innerchr20:12250448..12294236hg18UCSC Ensembl
Innerchr20:12250448..12294236hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843789
hg1943789
hg1843789
hg1743789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704553
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528024
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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