A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021168



Internal ID20588208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76088476..76089295hg38UCSC Ensembl
chr14:76554819..76555638hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492697
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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