A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456803



Internal ID21114356
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 StatusM
Merged Variants
Supporting Variantsnssv17987747
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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