A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559585



Internal ID332615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5692740..5692857hg38UCSC Ensembl
chr19:5692751..5692868hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720849
Samples
Known GenesLONP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559585
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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