A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916640



Internal ID22691859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126661199..126661270hg38UCSC Ensembl
chr9:129423478..129423549hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447349
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916640
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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