A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944606



Internal ID22720073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27255214..27291525hg38UCSC Ensembl
chr19:27746122..27782433hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3836312
hg1936312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944606
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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