A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241832



Internal ID22046442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26996651..26996651hg38UCSC Ensembl
chr15:27241798..27241798hg19UCSC 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 Variantsnssv17846779
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241832
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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