A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943238



Internal ID22718684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45023880..45024104hg38UCSC Ensembl
chr19:45527138..45527362hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398190
Samples
Known GenesRELB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943238
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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