A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916843



Internal ID22692062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134026732..134055450hg38UCSC Ensembl
chr9:136891854..136920572hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3828719
hg1928719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432134
Samples
Known GenesBRD3, LINC00094
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916843
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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