A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390593



Internal ID21381728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34867115..34868364hg38UCSC Ensembl
chr13:35441252..35442501hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705540
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390593
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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