A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446468



Internal ID21104021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121365106..121365517hg38UCSC Ensembl
chr9:124127384..124127795hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176301
Samples
Known GenesSTOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446468
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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