A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112867



Internal ID21482737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26968726..26968726hg38UCSC Ensembl
chr2:27191594..27191594hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382490
hg192490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616377
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112867
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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