A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076866



Internal ID21409081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95322055..95322055hg38UCSC Ensembl
chr11:95055219..95055219hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660196
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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