A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247139



Internal ID22051749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62349719..62349719hg38UCSC Ensembl
chr10:64109478..64109478hg19UCSC Ensembl
Cytoband10q21.2
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 Variantsnssv17841916
Samples
Known GenesLOC283045
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247139
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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