A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240432



Internal ID22045042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17827410..17827410hg38UCSC Ensembl
chr10:17869409..17869409hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841862
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240432
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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