A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524130



Internal ID300338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53781630..53792664hg38UCSC Ensembl
chr17:51858991..51870025hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811035
hg1911035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524130
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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