A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047669



Internal ID99650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69039431..69039468hg38UCSC Ensembl
chr11:68806899..68806936hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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