A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465483



Internal ID21123036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90247910..90876000hg38UCSC Ensembl
chr11:89981078..90609168hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38628091
hg19628091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996407
Samples
Known GenesDISC1FP1, MIR4490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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