A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028177



Internal ID21937520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70336398..70357434hg38UCSC Ensembl
chr14:70803115..70824151hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3821037
hg1921037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599977
Samples
Known GenesCOX16, SYNJ2BP-COX16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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