A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941469



Internal ID22716893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35045650..35045718hg38UCSC Ensembl
chr19:35536554..35536622hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406668
Samples
Known GenesHPN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941469
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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