A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437346



Internal ID21094899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128821693..128822783hg38UCSC Ensembl
chr9:131583972..131585062hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176918
Samples
Known GenesC9orf114, ENDOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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