A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046579



Internal ID98863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61700342..61700355hg38UCSC Ensembl
chr11:61467814..61467827hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547112
Supporting Variants
Samples
Known GenesDAGLA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046579
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02966


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