A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178940



Internal ID20745980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133101121..133186349hg38UCSC Ensembl
chr12:133677707..133762935hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3885229
hg1985229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480301
Supporting Variants
Samples
Known GenesZNF10, ZNF140, ZNF268, ZNF891
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178940
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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