A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559789



Internal ID18858070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80613653..80638520hg38UCSC Ensembl
Innerchr16:80647550..80672417hg19UCSC Ensembl
Innerchr16:79205051..79229918hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3824868
hg1924868
hg1824868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055196
Supporting Variants
Samples
Known GenesCDYL2, MIR548H4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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