A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064931



Internal ID20631971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89533526..89538042hg38UCSC Ensembl
chr1:89999085..90003601hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg384517
hg194517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334204
Supporting Variants
Samples
Known GenesLRRC8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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