A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094028



Internal ID20661068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141031770..141039928hg38UCSC Ensembl
chr3:140750612..140758770hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg388159
hg198159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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