A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066965



Internal ID18809496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76624313..77688151hg38UCSC Ensembl
Innerchr16:76658210..77722048hg19UCSC Ensembl
Innerchr16:75215711..76279549hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381063839
hg191063839
hg181063839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3027n100
Supporting Variantsnssv3559651
Samples
Known GenesADAMTS18, MIR4719, MON1B, SYCE1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066965
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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