A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987747



Internal ID20554787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129870441..129872825hg38UCSC Ensembl
chr11:129740336..129742720hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382385
hg192385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456803
Supporting Variants
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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