A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664778



Internal ID21613085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152208990..152251507hg38UCSC Ensembl
chr1:152181466..152223983hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3842518
hg1942518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060809
Samples
Known GenesHRNR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664778
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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