A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034090



Internal ID21943433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34784568..34784691hg38UCSC Ensembl
chr14:35253774..35253897hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598050
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034090
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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