A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046598



Internal ID98876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61975453..61975504hg38UCSC Ensembl
chr11:61742925..61742976hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046598
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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