A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801814



Internal ID21247152
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 StatusM
Merged Variants
Supporting Variantsnssv13681532
Samples
Known GenesTRNAU1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801814
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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