A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240517



Internal ID22045127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28601412..28601412hg38UCSC Ensembl
chr10:28890341..28890341hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842093
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240517
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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