A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911291



Internal ID22686504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103566401..103569429hg38UCSC Ensembl
chr9:106328683..106331711hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383029
hg193029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911291
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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