A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927339



Internal ID22702567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33379484..33389966hg38UCSC Ensembl
chr9:33379482..33389964hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810483
hg1910483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444650
Samples
Known GenesAQP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927339
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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