A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986583



Internal ID20553623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108124344..108127304hg38UCSC Ensembl
chr11:107995071..107998031hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382961
hg192961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464772
Supporting Variants
Samples
Known GenesACAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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