A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060829



Internal ID19150048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60990189..61014989hg38UCSC Ensembl
Innerchr20:59565245..59590045hg19UCSC Ensembl
Innerchr20:58998640..59023440hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3824801
hg1924801
hg1824801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3584346
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)nsv1060829
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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