A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608707



Internal ID21557012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28571786..28571786hg38UCSC Ensembl
chr1:28898298..28898298hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064687
SamplesHG00731
Known GenesTRNAU1AP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608707
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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