A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373827



Internal ID21031380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119548194..119561112hg38UCSC Ensembl
chr3:119267041..119279959hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3812919
hg1912919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094557
Samples
Known GenesCD80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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