A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022076



Internal ID20589117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85968736..85973921hg38UCSC Ensembl
chr14:86435080..86440265hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg385186
hg195186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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