A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062079



Internal ID19151298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14353704..14449174hg38UCSC Ensembl
Innerchr20:14334350..14429820hg19UCSC Ensembl
Innerchr20:14282350..14377820hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3895471
hg1995471
hg1895471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4249n100
Supporting Variantsnssv3734880, nssv3734881
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062079
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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