A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747419



Internal ID20523438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106581844..106854530hg38UCSC Ensembl
chr14:107037830..107262745hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38272687
hg19224916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747419
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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