A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033969



Internal ID21943312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27461269..27464331hg38UCSC Ensembl
chr13:28035406..28038468hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg383063
hg193063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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