A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149391



Internal ID21506465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86430829..86430829hg38UCSC Ensembl
chr8:87443058..87443058hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636762
Supporting Variants
SamplesNA19983
Known GenesWWP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149391
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