A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098105



Internal ID20665145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167335019..167335339hg38UCSC Ensembl
chr3:167052807..167053127hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359463
Supporting Variants
Samples
Known GenesZBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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