A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705754



Internal ID21378030
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 StatusS
Merged Variantsnsv4391056
Supporting Variants
Samples
Known GenesGNG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705754
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0948276


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