A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046424



Internal ID98750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70277061..70277109hg38UCSC Ensembl
chr11:70123167..70123215hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552390
Supporting Variants
Samples
Known GenesPPFIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046424
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.088952


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