A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013799



Internal ID21923142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:101655496..102001166hg38UCSC Ensembl
chr5:100991200..101336870hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38345671
hg19345671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013799
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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