A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075435



Internal ID21462827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66249470..66249470hg38UCSC Ensembl
chr11:66016941..66016941hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645636
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075435
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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