A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053770



Internal ID103686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131195627..131196622hg38UCSC Ensembl
chr11:131065522..131066517hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053770
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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