A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266278



Internal ID20475496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26345008..26345059hg38UCSC Ensembl
chr1:26671499..26671550hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731897
Supporting Variants
Samples
Known GenesAIM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266278
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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