A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459070



Internal ID237089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148147180..148148341hg38UCSC Ensembl
chr5:147526743..147527904hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459070
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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