A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143042



Internal ID20710082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166449701..166451100hg38UCSC Ensembl
chr6:166863189..166864588hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608801
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0006


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