A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913564



Internal ID22688780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77980493..77980569hg38UCSC Ensembl
chr10:79740251..79740327hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364452
Samples
Known GenesPOLR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913564
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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