A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526285



Internal ID21850643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12575972..12634788hg38UCSC Ensembl
chr1:12636000..12694793hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3858817
hg1958794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980904
Supporting Variants
Samples
Known GenesDHRS3, MIR6730
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526285
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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