A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448863



Internal ID227119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160177660..160182082hg38UCSC Ensembl
chr3:159895447..159899869hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384423
hg194423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940164
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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