A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059059



Internal ID18801590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7793987..8053708hg38UCSC Ensembl
Innerchr20:7774634..8034355hg19UCSC Ensembl
Innerchr20:7722634..7982355hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38259722
hg19259722
hg18259722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599364
Samples
Known GenesHAO1, TMX4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059059
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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