A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995577



Internal ID21904920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166716570..166722056hg38UCSC Ensembl
chr4:167637721..167643207hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385487
hg195487
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995577
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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