A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907839



Internal ID22683049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128044411..128058880hg38UCSC Ensembl
chr9:130806690..130821159hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814470
hg1914470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907839
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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