A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028518



Internal ID21937861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89337221..89396245hg38UCSC Ensembl
chr13:89989475..90048499hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3859025
hg1959025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028518
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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