A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027109



Internal ID21936452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106956336..106956412hg38UCSC Ensembl
chr13:107608684..107608760hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027109
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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