A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859707



Internal ID22634642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33379590..33389759hg38UCSC Ensembl
chr9:33379588..33389757hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810170
hg1910170
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512966
Samples
Known GenesAQP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859707
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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