A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997821



Internal ID21907164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58189924..58191217hg38UCSC Ensembl
chr4:59056090..59057383hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381294
hg191294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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