A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531591



Internal ID21855947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202458026..202458026hg38UCSC Ensembl
chr1:202427154..202427154hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050441
Supporting Variants
Samples
Known GenesPPP1R12B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531591
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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