A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114265



Internal ID21512702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43415974..43436663hg38UCSC Ensembl
chr2:43643113..43663802hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3820690
hg1920690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667853
Supporting Variants
Samples
Known GenesTHADA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114265
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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