A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671337



Internal ID21619642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33684430..33694208hg38UCSC Ensembl
chr6:33652207..33661985hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389779
hg199779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150195
SamplesNA19239
Known GenesITPR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671337
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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