A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473299



Internal ID21130852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91482462..91483544hg38UCSC Ensembl
chr11:91215628..91216710hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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