A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556990



Internal ID21881345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78707017..78711006hg38UCSC Ensembl
chr3:78756167..78760156hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383990
hg193990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994082
Supporting Variants
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556990
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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