A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094359



Internal ID20661399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142624289..142636952hg38UCSC Ensembl
chr3:142343131..142355794hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3812664
hg1912664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375226
Supporting Variants
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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