A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456375



Internal ID21113928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106426352..106467111hg38UCSC Ensembl
chr11:106297079..106337838hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3840760
hg1940760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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