A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466727



Internal ID244558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26504095..26504558hg38UCSC Ensembl
chr5:26504204..26504667hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466727
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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