A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029529



Internal ID21938872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99408588..99409522hg38UCSC Ensembl
chr14:99874925..99875859hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614989
Samples
Known GenesSETD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029529
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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