A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874472



Internal ID22649424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1600600..1608287hg38UCSC Ensembl
chr19:1600599..1608286hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387688
hg197688
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473282
Samples
Known GenesUQCR11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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