A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459799



Internal ID21117352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62375900..62407193hg38UCSC Ensembl
chr11:62143372..62174665hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3831294
hg1931294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188103
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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