A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093969



Internal ID20661009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13998993..14018507hg38UCSC Ensembl
chr3:14040493..14060007hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3819515
hg1919515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370446
Supporting Variants
Samples
Known GenesTPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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