A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241823



Internal ID22046433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25922227..25922227hg38UCSC Ensembl
chr15:26167374..26167374hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846771
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241823
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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