A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830856



Internal ID22605791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97420771..97426003hg38UCSC Ensembl
chr1:97886327..97891559hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385233
hg195233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481604
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830856
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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