A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072581



Internal ID21488684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121185795..121185795hg38UCSC Ensembl
chr11:121056504..121056504hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649920
Supporting Variants
SamplesNA18939
Known GenesTECTA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072581
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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