A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044961



Internal ID97721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43641084..43641120hg38UCSC Ensembl
chr11:43662634..43662670hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001717


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