A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092741



Internal ID20659781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114288001..114296300hg38UCSC Ensembl
chr3:114006848..114015147hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361653
Supporting Variants
Samples
Known GenesTIGIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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