A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249831



Internal ID22054441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74589049..74589049hg38UCSC Ensembl
chr15:74881390..74881390hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848661
Samples
Known GenesARID3B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249831
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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