A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730843



Internal ID20506758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111044304..111044372hg38UCSC Ensembl
chr9:113806584..113806652hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730843
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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