A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938196



Internal ID22713574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48776959..48789762hg38UCSC Ensembl
chr19:49280216..49293019hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3812804
hg1912804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938196
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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