A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589941



Internal ID18888222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:80652..96321hg38UCSC Ensembl
Innerchr20:61293..76962hg19UCSC Ensembl
Innerchr20:9293..24962hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3815670
hg1915670
hg1815670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067152
Supporting Variants
Samples
Known GenesDEFB125
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589941
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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