A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526027



Internal ID21850385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23853383..23853436hg38UCSC Ensembl
chr1:24179873..24179926hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982960
Supporting Variants
Samples
Known GenesFUCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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