A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852154



Internal ID22627089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132080728..132085806hg38UCSC Ensembl
chr8:133092975..133098053hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385079
hg195079
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506890
Samples
Known GenesHHLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852154
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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