A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466088



Internal ID21123641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103447322..103593444hg38UCSC Ensembl
chr11:103318050..103464172hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38146123
hg19146123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193535
Samples
Known GenesDYNC2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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