A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260150



Internal ID22064760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189810118..189810118hg38UCSC Ensembl
chr3:189527907..189527907hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17853602
Samples
Known GenesTP63
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260150
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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