A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727101



Internal ID150767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42919215..42921486hg38UCSC Ensembl
chr21:44339325..44341596hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382272
hg192272
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727101
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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