A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980781



Internal ID21890124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116122785..116122900hg38UCSC Ensembl
chr1:116665406..116665521hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519651
Samples
Known GenesMAB21L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980781
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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