A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063731



Internal ID18806262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70018481..70164481hg38UCSC Ensembl
Innerchr16:70052384..70198384hg19UCSC Ensembl
Innerchr16:68609885..68755885hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38146001
hg19146001
hg18146001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3007n100
Supporting Variantsnssv3722744
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)nsv1063731
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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