A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858387



Internal ID22633322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78550156..78554810hg38UCSC Ensembl
chr8:79462391..79467045hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg384655
hg194655
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509933, nssv17509932
Samples
Known GenesPKIA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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