A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072830



Internal ID21413280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116687997..116687997hg38UCSC Ensembl
chr11:116558713..116558713hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655834
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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