A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027704



Internal ID21937047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33646992..33650242hg38UCSC Ensembl
chr13:34221129..34224379hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602137
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027704
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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