A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243063



Internal ID21311647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4054960..4142615hg38UCSC Ensembl
Outerchr3:4053291..4143342hg38UCSC Ensembl
Innerchr3:4096644..4184299hg19UCSC Ensembl
Outerchr3:4094975..4185026hg19UCSC Ensembl
Innerchr3:4071644..4159299hg18UCSC Ensembl
Outerchr3:4069975..4160026hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3890052
hg1990052
hg1890052
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169507
Supporting Variants
SamplesSNI_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243063
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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