A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458698



Internal ID21116251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80095545..80107622hg38UCSC Ensembl
chr11:79806589..79818666hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3812078
hg1912078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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