A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460351



Internal ID238339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152216621..152216998hg38UCSC Ensembl
chr5:151596182..151596559hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460351
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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