A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882042



Internal ID22657019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35403506..35404555hg38UCSC Ensembl
chr19:35894408..35895457hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882042
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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