A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562371



Internal ID335328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46418429..46425150hg38UCSC Ensembl
chr19:46921686..46928407hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386722
hg196722
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562371
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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