A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260968



Internal ID22065578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165478596..165478596hg38UCSC Ensembl
chr6:165892084..165892084hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858063
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260968
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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