A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063761



Internal ID18806292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80606381..80629768hg38UCSC Ensembl
Innerchr16:80640278..80663665hg19UCSC Ensembl
Innerchr16:79197779..79221166hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3823388
hg1923388
hg1823388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3043n100
Supporting Variantsnssv3559788
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)nsv1063761
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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