A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247443



Internal ID22052053
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 StatusM
Merged Variants
Supporting Variantsnssv17842620
Samples
Known GenesPPRC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247443
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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