A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273584



Internal ID20482802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42181797..42181863hg38UCSC Ensembl
chr1:42647468..42647534hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747227
Supporting Variants
Samples
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273584
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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