A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111296



Internal ID21475875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220582527..220582527hg38UCSC Ensembl
chr2:221447248..221447248hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618213
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111296
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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