A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059097



Internal ID20626137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24175861..24178156hg38UCSC Ensembl
chr1:24502351..24504646hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382296
hg192296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321264
Supporting Variants
Samples
Known GenesIFNLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059097
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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