A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445028



Internal ID223388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82419345..82424394hg38UCSC Ensembl
chr3:82468496..82473545hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445028
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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