A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053291



Internal ID103377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122182858..122182895hg38UCSC Ensembl
chr11:122053566..122053603hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545845
Supporting Variants
Samples
Known GenesMIR100HG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053291
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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