A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944824



Internal ID21364893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102541898..102541898hg38UCSC Ensembl
chr8:103554126..103554126hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382327
hg192327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204661
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944824
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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