A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022367



Internal ID20589407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86903600..86905728hg38UCSC Ensembl
chr14:87369944..87372072hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492876
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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