A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113150



Internal ID21296416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9166640..9179255hg38UCSC Ensembl
Innerchr19:9277316..9289931hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812616
hg1912616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv548n145
Supporting Variantsnssv14101482, nssv14101196, nssv14101155, nssv14101114, nssv14100366, nssv14100992, nssv14099025, nssv14101343, nssv14100325
Samplessample70, sample359, sample423, sample4, sample143, sample157, sample299, sample55, sample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113150
Frequency
Sample Size467
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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