A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466185



Internal ID21123738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121807922..121832530hg38UCSC Ensembl
chr11:121678630..121703238hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3824609
hg1924609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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