A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249819



Internal ID22054429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72594838..72594838hg38UCSC Ensembl
chr15:72887179..72887179hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249819
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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