A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049996



Internal ID101227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94641843..94647162hg38UCSC Ensembl
chr11:94375009..94380328hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049996
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008432


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