A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731918



Internal ID20507839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16332320..16332428hg38UCSC Ensembl
chr9:16332318..16332426hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731918
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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