A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557436



Internal ID330533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32091133..32093655hg38UCSC Ensembl
chr19:32582039..32584561hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382523
hg192523
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557436
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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