A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247597



Internal ID22052207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118551107..118551107hg38UCSC Ensembl
chr10:120310619..120310619hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247597
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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