A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058640



Internal ID19147859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57932354..58214787hg38UCSC Ensembl
Innerchr20:56507410..56789843hg19UCSC Ensembl
Innerchr20:55940816..56223249hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38282434
hg19282434
hg18282434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584244
Samples
Known GenesC20orf85
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058640
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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