A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100559



Internal ID20667599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18964581..18964862hg38UCSC Ensembl
chr3:19006073..19006354hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0163


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