A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022943



Internal ID20589983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94566896..94569911hg38UCSC Ensembl
chr14:95033233..95036248hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513953
Supporting Variants
Samples
Known GenesSERPINA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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