A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022477



Internal ID20589517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96883901..96886200hg38UCSC Ensembl
chr14:97350238..97352537hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505752
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0011


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