A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873145



Internal ID22648089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48758730..48761129hg38UCSC Ensembl
chr20:47375267..47377666hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486092
Samples
Known GenesPREX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873145
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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