A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261979



Internal ID20471197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68868424..68868539hg38UCSC Ensembl
chr14:69335141..69335256hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261979
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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