A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182806



Internal ID20749846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21448239..21462435hg38UCSC Ensembl
chr11:21469785..21483981hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3814197
hg1914197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441802
Supporting Variants
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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