A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936494



Internal ID22711849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33613710..33615331hg38UCSC Ensembl
chr19:34104616..34106237hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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