A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263795



Internal ID20473013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58316896..58317075hg38UCSC Ensembl
chr14:58783614..58783793hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743888
Supporting Variants
Samples
Known GenesARID4A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263795
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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