A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423079



Internal ID21080632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23337115..23400016hg38UCSC Ensembl
chr9:23337113..23400014hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3862902
hg1962902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7649n223
Supporting Variantsnssv18222361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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