A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453100



Internal ID21110653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126766838..126782878hg38UCSC Ensembl
chr9:129529117..129545157hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3816041
hg1916041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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