A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054816



Internal ID104380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:135056364..135076500hg38UCSC Ensembl
chr11:134926258..134946394hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3820137
hg1920137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054816
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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