A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851957



Internal ID22626892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78564130..78575391hg38UCSC Ensembl
chr8:79476365..79487626hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3811262
hg1911262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509935
Samples
Known GenesPKIA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851957
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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