A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880718



Internal ID22655688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29036274..29040914hg38UCSC Ensembl
chr19:29527181..29531821hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384641
hg194641
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880718
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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