A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453634



Internal ID21111187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89900478..89910390hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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