A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065195



Internal ID19154414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60986624..61015133hg38UCSC Ensembl
Innerchr20:59561680..59590189hg19UCSC Ensembl
Innerchr20:58995075..59023584hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3828510
hg1928510
hg1828510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3584331, nssv3584334, nssv3584332, nssv3584330, nssv3584329, nssv3584333
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065195
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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