A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050186



Internal ID101361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111098185..111100320hg38UCSC Ensembl
chr11:110968909..110971044hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382136
hg192136
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050186
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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