A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249978



Internal ID22054588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95325633..95325633hg38UCSC Ensembl
chr15:95868862..95868862hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847180
Samples
Known GenesLOC400456
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249978
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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