A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391056



Internal ID21379635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51911626..51912184hg38UCSC Ensembl
chr14:52378344..52378902hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705754
Samples
Known GenesGNG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391056
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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