A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559787



Internal ID18511382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80606381..80629195hg38UCSC Ensembl
Innerchr16:80640278..80663092hg19UCSC Ensembl
Innerchr16:79197779..79220593hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3822815
hg1922815
hg1822815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063971
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)nssv3559787
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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