A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106989



Internal ID21480943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10100996..10100996hg38UCSC Ensembl
chr2:10241123..10241123hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606702
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106989
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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