A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029020



Internal ID21938363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70580454..70582572hg38UCSC Ensembl
chr14:71047171..71049289hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029020
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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