A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022190



Internal ID20589231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94949101..94951700hg38UCSC Ensembl
chr14:95415438..95418037hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00655


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