A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454593



Internal ID232691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61191746..61195685hg38UCSC Ensembl
chr5:60487573..60491512hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454593
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer