A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016891



Internal ID20583932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25765621..25766210hg38UCSC Ensembl
chr14:26234827..26235416hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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