A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515898



Internal ID292371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55738331..55740555hg38UCSC Ensembl
chr17:53815692..53817916hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg382225
hg192225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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