A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560001



Internal ID333019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2158209..2161290hg38UCSC Ensembl
chr19:2158208..2161289hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383082
hg193082
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560001
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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