A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114611



Internal ID21495425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60735763..60735763hg38UCSC Ensembl
chr2:60962898..60962898hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609310
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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