A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102254



Internal ID20669294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66457440..66459569hg38UCSC Ensembl
chr3:66507864..66509993hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356721
Supporting Variants
Samples
Known GenesLRIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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