A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020718



Internal ID20587758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65120301..65126400hg38UCSC Ensembl
chr14:65587019..65593118hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491434
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00293


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