A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995594



Internal ID21904937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119062319..119081694hg38UCSC Ensembl
chr4:119983474..120002849hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3819376
hg1919376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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