A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841655



Internal ID22025298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45984922..45984922hg38UCSC Ensembl
chr10:51610912..51610912hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240631
Supporting Variants
Samples
Known GenesTIMM23
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841655
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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