A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094281



Internal ID20661321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141041494..141046354hg38UCSC Ensembl
chr3:140760336..140765196hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384861
hg194861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00184


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