A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026293



Internal ID21935636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73474167..73481630hg38UCSC Ensembl
chr14:73940872..73948335hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387464
hg197464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605751
Samples
Known GenesHEATR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026293
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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