A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065118



Internal ID18807649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69994778..70163852hg38UCSC Ensembl
Innerchr16:70028681..70197755hg19UCSC Ensembl
Innerchr16:68586182..68755256hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38169075
hg19169075
hg18169075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3007n100
Supporting Variantsnssv3559487
Samples
Known GenesMIR1972-1, 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)nsv1065118
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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