A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563573



Internal ID336505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49073600..49079993hg38UCSC Ensembl
chr15:49365797..49372190hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg386394
hg196394
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563573
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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