A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712188



Internal ID135854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21637879..22065420hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38427542
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712188
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.487043


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