A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991709



Internal ID21901052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160071938..160072049hg38UCSC Ensembl
chr3:159789725..159789836hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539423
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991709
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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