A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455540



Internal ID21113093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78010940..78018818hg38UCSC Ensembl
chr10:79770698..79778576hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984355
Samples
Known GenesPOLR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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