A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260076



Internal ID20469294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59975054..59975116hg38UCSC Ensembl
chr14:60441772..60441834hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742022
Supporting Variants
Samples
Known GenesLRRC9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260076
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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