A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943997



Internal ID21364066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58593944..58594269hg38UCSC Ensembl
chr1:59059616..59059941hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15182982
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943997
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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