A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874474



Internal ID22649426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43638473..43640972hg38UCSC Ensembl
chr20:42267113..42269612hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486026
Samples
Known GenesIFT52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874474
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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