A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401452



Internal ID180829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58630000..58630051hg38UCSC Ensembl
chr1:59095672..59095723hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401452
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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