A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019877



Internal ID20586917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58199801..58200400hg38UCSC Ensembl
chr14:58666519..58667118hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479571
Supporting Variants
Samples
Known GenesACTR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08278


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