A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614795



Internal ID21806842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53466161..53476243hg38UCSC Ensembl
chr14:53932879..53942961hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3810083
hg1910083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614795
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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