A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445209



Internal ID223566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74913135..74920374hg38UCSC Ensembl
chr3:74962286..74969525hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg387240
hg197240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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