A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391118



Internal ID21379697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71068636..71068839hg38UCSC Ensembl
chr14:71535353..71535556hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705789
Samples
Known GenesPCNX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391118
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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