A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486289



Internal ID21143842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66399066..66399727hg38UCSC Ensembl
chr14:66865784..66866445hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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