A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874818



Internal ID22649772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53628752..53630351hg38UCSC Ensembl
chr20:52245291..52246890hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874818
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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