A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463228



Internal ID21120781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102540187..102550285hg38UCSC Ensembl
chr11:102410918..102421016hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3810099
hg1910099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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