A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249972



Internal ID22054582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94900402..94900402hg38UCSC Ensembl
chr15:95443631..95443631hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249972
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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