A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107800



Internal ID21482332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102002782..102002782hg38UCSC Ensembl
chr2:102619244..102619244hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610026
Supporting Variants
SamplesHG03732
Known GenesIL1R2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107800
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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