A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611346



Internal ID21803393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64379655..64381539hg38UCSC Ensembl
chr14:64846373..64848257hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381885
hg191885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034009
Supporting Variants
Samples
Known GenesMIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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