A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874898



Internal ID22649852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3064591..3070465hg38UCSC Ensembl
chr19:3064589..3070463hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385875
hg195875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874898
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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