A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252468



Internal ID22057078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58436296..58436296hg38UCSC Ensembl
chr2:58663431..58663431hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252468
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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