A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914182



Internal ID22689399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135615200..135615264hg38UCSC Ensembl
chr9:138507046..138507110hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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