A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532721



Internal ID308634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57071076..57071502hg38UCSC Ensembl
chr17:55148437..55148863hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532721
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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