A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875415



Internal ID22650372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21305644..21308111hg38UCSC Ensembl
chr20:21286282..21288749hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382468
hg192468
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483270
Samples
Known GenesXRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875415
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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