A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113517



Internal ID21296783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208551333..208565337hg38UCSC Ensembl
Innerchr1:208724678..208738682hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3814005
hg1914005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109026
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113517
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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