A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449890



Internal ID21107443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114918819..114920116hg38UCSC Ensembl
chr9:117681099..117682396hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175085
Samples
Known GenesTNFSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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