A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053553



Internal ID103549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132314828..132337966hg38UCSC Ensembl
chr11:132184722..132207860hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3823139
hg1923139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513063
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053553
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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