A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052026



Internal ID20619066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154449989..154453030hg38UCSC Ensembl
chr1:154422465..154425506hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383042
hg193042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332009
Supporting Variants
Samples
Known GenesIL6R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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