A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031840



Internal ID21941183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84160139..84660831hg38UCSC Ensembl
chr13:84734274..85234966hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38500693
hg19500693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617218
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031840
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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