A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042077



Internal ID95754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1499399..1499577hg38UCSC Ensembl
chr11:1520629..1520807hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509939
Supporting Variants
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042077
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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