A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072542



Internal ID21512760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115325113..115346068hg38UCSC Ensembl
chr11:115195832..115216787hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3820956
hg1920956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665657
Supporting Variants
Samples
Known GenesCADM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072542
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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