A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444168



Internal ID21101721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18076001..18081400hg38UCSC Ensembl
chr11:18097548..18102947hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193348
Samples
Known GenesSAAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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