A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110629



Internal ID21465329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18276630..18276630hg38UCSC Ensembl
chr2:18457896..18457896hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609433
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110629
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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