A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732438



Internal ID20508362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23853353..23853454hg38UCSC Ensembl
chr1:24179843..24179944hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279957
Samples
Known GenesFUCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732438
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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