A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935967



Internal ID21356036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234669966..234669966hg38UCSC Ensembl
chr1:234805712..234805712hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190273
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935967
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