A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048275



Internal ID100054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72609864..72609864hg38UCSC Ensembl
chr11:72320908..72320908hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5402263
Supporting Variants
Samples
Known GenesPDE2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048275
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.217768


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