A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623219



Internal ID21571524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86858906..86858906hg38UCSC Ensembl
chr2:87086029..87086029hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114926
SamplesHG03683
Known GenesCD8B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623219
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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