A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441802



Internal ID21099355
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 StatusM
Merged Variants
Supporting Variantsnssv18182806
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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