A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247794



Internal ID22052404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14348082..14348082hg38UCSC Ensembl
chr11:14369628..14369628hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842525
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247794
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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