A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021387



Internal ID21930730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21990935..22478874hg38UCSC Ensembl
chr14:22459174..22947863hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38487940
hg19488690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021387
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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