A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843007



Internal ID22026650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113133047..113133047hg38UCSC Ensembl
chr10:114892806..114892806hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247534
Supporting Variants
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843007
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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