A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031520



Internal ID21940863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34784242..34784325hg38UCSC Ensembl
chr14:35253448..35253531hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605033
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031520
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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