A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447528



Internal ID21105081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82745425..82747029hg38UCSC Ensembl
chr9:85360340..85361944hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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