A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027068



Internal ID21936411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36511639..36511703hg38UCSC Ensembl
chr14:36980844..36980908hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600724
Samples
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027068
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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