A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842585



Internal ID22026228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61377742..61377742hg38UCSC Ensembl
chr11:61145214..61145214hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842585
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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