A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681532



Internal ID21203398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28571787..28571787hg38UCSC Ensembl
chr1:28898299..28898299hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801814
Supporting Variants
Samples
Known GenesTRNAU1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681532
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.112903


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