A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466022



Internal ID243872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162739924..162741181hg38UCSC Ensembl
chr5:162166930..162168187hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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