A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092742



Internal ID20659782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114309407..114310271hg38UCSC Ensembl
chr3:114028254..114029118hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359670
Supporting Variants
Samples
Known GenesTIGIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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