A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586518



Internal ID21535072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5709838..5709893hg38UCSC Ensembl
chr19:5709849..5709904hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106454
SamplesHG02011
Known GenesLONP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586518
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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