A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241313



Internal ID22045923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28264721..28264721hg38UCSC Ensembl
chr1:28591232..28591232hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17844160
Samples
Known GenesSESN2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241313
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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