A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066640



Internal ID19155859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:80652..94828hg38UCSC Ensembl
Innerchr20:61293..75469hg19UCSC Ensembl
Innerchr20:9293..23469hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3814177
hg1914177
hg1814177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4218n100
Supporting Variantsnssv3589940
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)nsv1066640
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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