A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029139



Internal ID21938482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36879468..36879684hg38UCSC Ensembl
chr13:37453605..37453821hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602391
Samples
Known GenesSMAD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029139
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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