A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612871



Internal ID21561176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3694003..3694003hg38UCSC Ensembl
chr1:3610567..3610567hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065026
SamplesNA19238
Known GenesTP73
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612871
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer