A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110727



Internal ID21468022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17852992..17852992hg38UCSC Ensembl
chr2:18034259..18034259hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620535
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110727
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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