A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240326



Internal ID22044936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3662733..3662733hg38UCSC Ensembl
chr10:3704925..3704925hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240326
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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