A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240417



Internal ID22045027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14897734..14897734hg38UCSC Ensembl
chr10:14939733..14939733hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841847
Samples
Known GenesSUV39H2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240417
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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