A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241822



Internal ID22046432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25917352..25917352hg38UCSC Ensembl
chr15:26162499..26162499hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846770
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241822
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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