A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743127



Internal ID20519113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75407796..75408636hg38UCSC Ensembl
chr14:75874499..75875339hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743127
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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