A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474687



Internal ID21132240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93268001..93277400hg38UCSC Ensembl
chr11:93001167..93010566hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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