A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994879



Internal ID21904222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119210350..119211834hg38UCSC Ensembl
chr4:120131505..120132989hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381485
hg191485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994879
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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