A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842620



Internal ID22026263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102134699..102134699hg38UCSC Ensembl
chr10:103894456..103894456hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247443
Supporting Variants
Samples
Known GenesPPRC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842620
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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