A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460245



Internal ID21117798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107654301..108069600hg38UCSC Ensembl
chr11:107525027..107940327hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38415300
hg19415301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1303n223
Supporting Variantsnssv18193738
Samples
Known GenesCUL5, ELMOD1, RAB39A, SLC35F2, SLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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