A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003326



Internal ID21912669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15537827..15548887hg38UCSC Ensembl
chr6:15538058..15549118hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3811061
hg1911061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569681
Samples
Known GenesDTNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003326
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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