A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112744



Internal ID21466920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25041603..25041603hg38UCSC Ensembl
chr2:25264472..25264472hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611803
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112744
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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