A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046734



Internal ID19135953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19932666..19954015hg38UCSC Ensembl
Innerchr16:19943988..19965337hg19UCSC Ensembl
Innerchr16:19851489..19872838hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821350
hg1921350
hg1821350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2789n100
Supporting Variantsnssv3542837
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046734
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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