A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010113



Internal ID21919456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60568630..60569142hg38UCSC Ensembl
chr9_gl000199_random:50072..50584hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010113
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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