A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739478



Internal ID20515451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24333511..24336830hg38UCSC Ensembl
chr14:24802717..24806036hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383320
hg193320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293103
Samples
Known GenesADCY4, RIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739478
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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