A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424280



Internal ID203275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26334427..26335297hg38UCSC Ensembl
chr1:26660918..26661788hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902454
Samples
Known GenesAIM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424280
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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