A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260375



Internal ID22064985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58919748..58919748hg38UCSC Ensembl
chr5:58215575..58215575hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260375
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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