A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880152



Internal ID22655122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3806383..3809394hg38UCSC Ensembl
chr20:3787030..3790041hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383012
hg193012
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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