A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403229



Internal ID182592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75736514..75736559hg38UCSC Ensembl
chr1:76202199..76202244hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907420
Samples
Known GenesACADM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403229
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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