A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018716



Internal ID20585756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44764538..44765132hg38UCSC Ensembl
chr14:45233741..45234335hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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