A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461341



Internal ID239295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87147635..87147702hg38UCSC Ensembl
chr4:88068787..88068854hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461341
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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