A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877547



Internal ID22652512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51419802..51431815hg38UCSC Ensembl
chr19:51923056..51935069hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3812014
hg1912014
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877547
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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