A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073298



Internal ID21457751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132432517..132432517hg38UCSC Ensembl
chr11:132302411..132302411hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383095
hg193095
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663347
Supporting Variants
SamplesHG02587
Known GenesOPCML
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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