A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466579



Internal ID244411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17599600..17750548hg38UCSC Ensembl
chr5:17599709..17750657hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38150949
hg19150949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466579
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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