A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741437



Internal ID20517414
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 StatusM
Merged Variants
Supporting Variantsnssv16284033
Samples
Known GenesNOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741437
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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