A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065688



Internal ID19154907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60987482..61015133hg38UCSC Ensembl
Innerchr20:59562538..59590189hg19UCSC Ensembl
Innerchr20:58995933..59023584hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3827652
hg1927652
hg1827652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3584338, nssv3584337, nssv3584339, nssv3731496
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)nsv1065688
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer