A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027680



Internal ID21937023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23656910..23656972hg38UCSC Ensembl
chr14:24126119..24126181hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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