A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026116



Internal ID21935459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31369522..31371820hg38UCSC Ensembl
chr13:31943659..31945957hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382299
hg192299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026116
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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