A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861590



Internal ID22636525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128092098..128099536hg38UCSC Ensembl
chr8:129104344..129111782hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg387439
hg197439
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506819
Samples
Known GenesPVT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861590
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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