A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022736



Internal ID20589776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91181853..91183202hg38UCSC Ensembl
chr14:91648197..91649546hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504173
Supporting Variants
Samples
Known GenesC14orf159
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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