A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017426



Internal ID20584466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34635595..34698774hg38UCSC Ensembl
chr14:35104801..35167980hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3863180
hg1963180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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