A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444265



Internal ID222643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57706862..57728743hg38UCSC Ensembl
chr3:57692589..57714470hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3821882
hg1921882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444265
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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