A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874699



Internal ID22649652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42706809..42708466hg38UCSC Ensembl
chr22:43102815..43104472hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483608
Samples
Known GenesA4GALT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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