A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873595



Internal ID22648543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58546390..58549630hg38UCSC Ensembl
chr19:59057757..59060997hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479361
Samples
Known GenesTRIM28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873595
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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