A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466792



Internal ID21124345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65360555..65368667hg38UCSC Ensembl
chr11:65128026..65136138hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg388113
hg198113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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