A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058789



Internal ID18801320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69942118..70146310hg38UCSC Ensembl
Innerchr16:69976021..70180213hg19UCSC Ensembl
Innerchr16:68533522..68737714hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38204193
hg19204193
hg18204193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2997n100
Supporting Variantsnssv3559445
Samples
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058789
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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