A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931905



Internal ID22707195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58141446..58154547hg38UCSC Ensembl
chr15:58433645..58446746hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3813102
hg1913102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374437
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931905
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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