A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473417



Internal ID21130970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76819336..76836358hg38UCSC Ensembl
chr11:76530380..76547402hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3817023
hg1917023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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