A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970926



Internal ID22745861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32875502..32875502hg38UCSC Ensembl
chr20:31463308..31463308hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970926
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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