A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074931



Internal ID21509911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39456123..39456123hg38UCSC Ensembl
chr11:39477673..39477673hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653731
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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