A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610906



Internal ID21559211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233340751..233340751hg38UCSC Ensembl
chr2:234249397..234249397hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg388816
hg198816
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111881
SamplesHG02818
Known GenesSAG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610906
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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