A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099910



Internal ID20666950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42457806..42461609hg38UCSC Ensembl
chr3:42499298..42503101hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383804
hg193804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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