A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451855



Internal ID230023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151594498..151694111hg38UCSC Ensembl
chr3:151312286..151411899hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3899614
hg1999614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941181
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451855
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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