A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902454



Internal ID2447
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 StatusS
Merged Variantsnsv5424280
Supporting Variants
Samples
Known GenesAIM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902454
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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