A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447374



Internal ID21104927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69874892..69875733hg38UCSC Ensembl
chr9:72489808..72490649hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184254
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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