A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837001



Internal ID22611936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67598710..67653991hg38UCSC Ensembl
chr3:67649134..67704415hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3855282
hg1955282
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494639
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837001
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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