A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421834



Internal ID21079387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3648840..3664407hg38UCSC Ensembl
chr9:3648840..3664407hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3815568
hg1915568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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