A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670338



Internal ID21618645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40023258..40038716hg38UCSC Ensembl
chr21:41395185..41410643hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3815459
hg1915459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118616
Samples
Known GenesDSCAM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670338
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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