A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620733



Internal ID21569038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219270701..219270701hg38UCSC Ensembl
chr2:220135423..220135423hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383145
hg193145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111459
SamplesHG03125
Known GenesTUBA4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620733
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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