A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670010



Internal ID21618316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71568978..71579606hg38UCSC Ensembl
chr11:71280024..71290652hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810629
hg1910629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075964
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670010
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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