A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928749



Internal ID22703993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89516126..89518532hg38UCSC Ensembl
chr15:90059357..90061763hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389105
Samples
Known GenesLINC00928
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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