A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953155



Internal ID21373153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195047788..195047788hg38UCSC Ensembl
chr3:194768517..194768517hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188537
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953155
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