A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260977



Internal ID22065587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166830153..166830153hg38UCSC Ensembl
chr6:167243641..167243641hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858072
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260977
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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