A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267926



Internal ID20477144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171096470..171096573hg38UCSC Ensembl
chr1:171065611..171065714hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742470
Supporting Variants
Samples
Known GenesFMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267926
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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