A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112836



Internal ID21444317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242141116..242183528hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3842413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668631
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112836
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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