A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667374



Internal ID21615679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215962719..215963440hg38UCSC Ensembl
chr2:216827442..216828163hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110059
Samples
Known GenesMREG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667374
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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