A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451387



Internal ID21108940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108459979..108460617hg38UCSC Ensembl
chr9:111222259..111222897hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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