A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240624



Internal ID22045234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45377090..45377090hg38UCSC Ensembl
chr10:45872538..45872538hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841648
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240624
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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