A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465531



Internal ID243393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161564159..161564682hg38UCSC Ensembl
chr5:160991165..160991688hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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