A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021179



Internal ID20588219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76326538..76332379hg38UCSC Ensembl
chr14:76792881..76798722hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385842
hg195842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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