A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467982



Internal ID21125535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92613562..92618101hg38UCSC Ensembl
chr11:92346728..92351267hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384540
hg194540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995410
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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