A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247395



Internal ID22052005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95213264..95213264hg38UCSC Ensembl
chr10:96973021..96973021hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842427
Samples
Known GenesC10orf129
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247395
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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