A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668398



Internal ID21616703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71132056..71145558hg38UCSC Ensembl
chr10:72891813..72905315hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813503
hg1913503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071816
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668398
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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