A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462415



Internal ID21119968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103386814..103815020hg38UCSC Ensembl
chr11:103257542..103685748hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38428207
hg19428207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986144
Samples
Known GenesDYNC2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462415
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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