A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537837



Internal ID313034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128522761..128522781hg38UCSC Ensembl
chr11:128392656..128392676hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051665
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537837
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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