A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063466



Internal ID19152685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80193731..80326566hg38UCSC Ensembl
Innerchr16:80227628..80360463hg19UCSC Ensembl
Innerchr16:78785129..78917964hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38132836
hg19132836
hg18132836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559780
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)nsv1063466
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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