A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047969



Internal ID99843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63577320..63577320hg38UCSC Ensembl
chr11:63344792..63344792hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546958
Supporting Variants
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047969
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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