A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512966



Internal ID22570921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33379590..33389759hg38UCSC Ensembl
chr9:33379588..33389757hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810170
hg1910170
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859707
Supporting Variants
Samples
Known GenesAQP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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