A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030086



Internal ID21939429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98063982..98064930hg38UCSC Ensembl
chr13:98716236..98717184hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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