A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410226



Internal ID189543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74912549..74912600hg38UCSC Ensembl
chr11:74623594..74623645hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047180
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410226
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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