A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109613



Internal ID21488249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162936686..162936686hg38UCSC Ensembl
chr2:163793196..163793196hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610883
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109613
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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