A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444394



Internal ID222766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177450063..177450274hg38UCSC Ensembl
chr3:177167851..177168062hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943587
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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