A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448329



Internal ID21105882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98054303..98063987hg38UCSC Ensembl
chr9:100816585..100826269hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389685
hg199685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178558
Samples
Known GenesNANS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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