A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031402



Internal ID21940745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51772171..51772253hg38UCSC Ensembl
chr14:52238889..52238971hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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