A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561398



Internal ID334380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49250286..49251996hg38UCSC Ensembl
chr16:49284197..49285907hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561398
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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