A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830127



Internal ID22605062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67174339..67227910hg38UCSC Ensembl
chr1:67640022..67693593hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3853572
hg1953572
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481153
Samples
Known GenesIL23R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830127
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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