A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865478



Internal ID22640413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45349730..45379433hg38UCSC Ensembl
chr10:45845178..45874881hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3829704
hg1929704
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460962
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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