A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444986



Internal ID223348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82806692..82812051hg38UCSC Ensembl
chr3:82855843..82861202hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385360
hg195360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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