A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879441



Internal ID22654410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15026091..15029290hg38UCSC Ensembl
chr19:15136903..15140101hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383200
hg193199
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879441
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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