A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067426



Internal ID18809957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18365549..18645096hg38UCSC Ensembl
Innerchr20:18346193..18625740hg19UCSC Ensembl
Innerchr20:18294193..18573740hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38279548
hg19279548
hg18279548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4283n100
Supporting Variantsnssv3584644
Samples
Known GenesDTD1, DZANK1, LINC00493, LINC00851, MIR3192, POLR3F, RBBP9, SEC23B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067426
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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