A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072756



Internal ID21453989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118331112..118331112hg38UCSC Ensembl
chr11:118201827..118201827hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661786
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072756
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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