A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404363



Internal ID183716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197217322..197217373hg38UCSC Ensembl
chr2:198082046..198082097hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923624
Samples
Known GenesANKRD44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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