A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102739



Internal ID20669779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54922901..54925900hg38UCSC Ensembl
chr3:54956928..54959927hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368316
Supporting Variants
Samples
Known GenesCACNA2D3, LRTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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