A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562351



Internal ID335309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32759470..32760322hg38UCSC Ensembl
chr20:31347276..31348128hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562351
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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