A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456368



Internal ID234438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174910519..174910903hg38UCSC Ensembl
chr5:174337522..174337906hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456368
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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