A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094293



Internal ID20661333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141204900..141211323hg38UCSC Ensembl
chr3:140923742..140930165hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386424
hg196424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0012


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