A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559791



Internal ID18858072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80623069..80673951hg38UCSC Ensembl
Innerchr16:80656966..80707848hg19UCSC Ensembl
Innerchr16:79214467..79265349hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3850883
hg1950883
hg1850883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058764
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)nssv3559791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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