A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562985



Internal ID335924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1403255..1403264hg38UCSC Ensembl
chr20:1383899..1383908hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810
hg1910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562985
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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