A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037413



Internal ID21946756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26746918..26754939hg38UCSC Ensembl
chr13:27321055..27329076hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg388022
hg198022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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