A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559793



Internal ID18858074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80905793..80921496hg38UCSC Ensembl
Innerchr16:80939690..80955393hg19UCSC Ensembl
Innerchr16:79497191..79512894hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3815704
hg1915704
hg1815704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063397
Supporting Variants
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)nssv3559793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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