A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923284



Internal ID22698511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45418932..45420905hg38UCSC Ensembl
chr10:45914380..45916353hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362409
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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