A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842768



Internal ID22026411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67997232..67997232hg38UCSC Ensembl
chr11:67764703..67764703hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248164
Supporting Variants
Samples
Known GenesUNC93B1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842768
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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