A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881843



Internal ID22656819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32304874..32307073hg38UCSC Ensembl
chr20:30892677..30894876hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1324n209
Supporting Variantsnssv17485294
Samples
Known GenesKIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881843
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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