A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244608



Internal ID22049218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102610040..102610040hg38UCSC Ensembl
chr5:101945744..101945744hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857856
Samples
Known GenesLINC00491, LINC00492
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244608
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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