A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013446



Internal ID21922789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77702093..77702226hg38UCSC Ensembl
chr9:80317009..80317142hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013446
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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