A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908411



Internal ID22683621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81575515..81587330hg38UCSC Ensembl
chr9:84190430..84202245hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3811816
hg1911816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441972
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908411
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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