A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997277



Internal ID21906620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43264796..43272511hg38UCSC Ensembl
chr4:43266813..43274528hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg387716
hg197716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997277
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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