A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022126



Internal ID21931469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92741765..92742626hg38UCSC Ensembl
chr14:93208110..93208971hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598974
Samples
Known GenesLGMN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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