A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443381



Internal ID21100934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111558470..111567612hg38UCSC Ensembl
chr9:114320750..114329892hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg389143
hg199143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174596
Samples
Known GenesPTGR1, ZNF483
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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