A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996916



Internal ID20563956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110446751..110448842hg38UCSC Ensembl
chr12:110884556..110886647hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382092
hg192092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494052
Supporting Variants
Samples
Known GenesARPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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