A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454108



Internal ID232212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160156897..160159396hg38UCSC Ensembl
chr5:159583904..159586403hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454108
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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