A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495299



Internal ID21152852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132878833..133215167hg38UCSC Ensembl
chr12:133455419..133791753hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38336335
hg19336335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1747n223
Supporting Variantsnssv18178074
Samples
Known GenesCHFR, ZNF10, ZNF140, ZNF26, ZNF268, ZNF605, ZNF84, ZNF891
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495299
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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