A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019809



Internal ID20586849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57157388..57157857hg38UCSC Ensembl
chr14:57624106..57624575hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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