A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836398



Internal ID22611333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60933941..60941499hg38UCSC Ensembl
chr3:60919613..60927171hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg387559
hg197559
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493963
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836398
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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