A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872272



Internal ID22647211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58481256..58483511hg38UCSC Ensembl
chr19:58992623..58994878hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382256
hg192256
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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