A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859816



Internal ID22043459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110526352..110526352hg38UCSC Ensembl
chr6:110847555..110847555hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257022
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859816
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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