A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052659



Internal ID102962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129520862..129522763hg38UCSC Ensembl
chr11:129390757..129392658hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052659
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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