A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444469



Internal ID21102022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78850673..78866353hg38UCSC Ensembl
chr9:81465589..81481269hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3815681
hg1915681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7845n223
Supporting Variantsnssv18228584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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