A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247962



Internal ID22052572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34360141..34360141hg38UCSC Ensembl
chr11:34381688..34381688hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17844476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247962
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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