A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511251



Internal ID20884578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65984893..65986922hg38UCSC Ensembl
chr15:66277231..66279260hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178313
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511251
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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