A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016913



Internal ID20583954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26620090..26620595hg38UCSC Ensembl
chr14:27089296..27089801hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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