A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284033



Internal ID20493251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77416800..77416853hg38UCSC Ensembl
chr14:77883143..77883196hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741437
Supporting Variants
Samples
Known GenesNOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284033
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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