A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086453



Internal ID21455253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131100..131100hg38UCSC Ensembl
chr11:186341..186341hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653688
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086453
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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