A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991710



Internal ID21901053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160101172..160104962hg38UCSC Ensembl
chr3:159818959..159822749hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg383791
hg193791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550015
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991710
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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