A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439397



Internal ID21096950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86567974..86584681hg38UCSC Ensembl
chr9:89182889..89199596hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3816708
hg1916708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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