A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034794



Internal ID21944137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7025928..7031269hg38UCSC Ensembl
chr17:6929247..6934588hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg385342
hg195342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618436
Samples
Known GenesBCL6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034794
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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