A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440424



Internal ID21097977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21535374..21718724hg38UCSC Ensembl
chr11:21556920..21740270hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38183351
hg19183351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189514
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440424
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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