A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922080



Internal ID22697305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108180553..108180797hg38UCSC Ensembl
chr9:110942833..110943077hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922080
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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