A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445469



Internal ID21103022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21264418..21264838hg38UCSC Ensembl
chr11:21285964..21286384hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989266
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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