A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994322



Internal ID21903665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81858341..81858662hg38UCSC Ensembl
chr3:81907492..81907813hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994322
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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