A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037732



Internal ID21947075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66764463..66767721hg38UCSC Ensembl
chr15:67056801..67060059hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383259
hg193259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603793
Samples
Known GenesSMAD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037732
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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