A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612665



Internal ID21560970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68686301..68686301hg38UCSC Ensembl
chr2:68913433..68913433hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113588
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612665
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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