A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099906



Internal ID20666946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42389589..42399023hg38UCSC Ensembl
chr3:42431081..42440515hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389435
hg199435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370345
Supporting Variants
Samples
Known GenesLYZL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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