A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458183



Internal ID21115736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76790589..76792491hg38UCSC Ensembl
chr11:76501633..76503535hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381903
hg191903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994337
Samples
Known GenesTSKU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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