A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961636



Internal ID22736579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52066514..52080754hg38UCSC Ensembl
chr20:50683053..50697293hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3814241
hg1914241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961636
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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