A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415772



Internal ID195021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56916493..56916544hg38UCSC Ensembl
chr20:55491549..55491600hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415772
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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