A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059316



Internal ID20626356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23860601..23861300hg38UCSC Ensembl
chr1:24187091..24187790hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333117
Supporting Variants
Samples
Known GenesFUCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0003


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