A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455683



Internal ID21113236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92546978..92627208hg38UCSC Ensembl
chr11:92280144..92360374hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3880231
hg1980231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995397
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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