A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030714



Internal ID21940057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109382772..109382826hg38UCSC Ensembl
chr13:110035119..110035173hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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