A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047872



Internal ID99778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62739534..62740626hg38UCSC Ensembl
chr11:62507006..62508098hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047872
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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