A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451979



Internal ID21109532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64440801..64561500hg38UCSC Ensembl
chr9:69453219..69573918hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38120700
hg19120700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7780n223
Supporting Variantsnssv18220168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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