A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549060



Internal ID322759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24140987..24140987hg38UCSC Ensembl
chr1:24467477..24467477hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901173
Samples
Known GenesIL22RA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549060
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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