A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027382



Internal ID21936725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65984866..65984947hg38UCSC Ensembl
chr15:66277204..66277285hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604266
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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