A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169996



Internal ID21314057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66514883..66527245hg38UCSC Ensembl
Outerchr4:66512370..66530383hg38UCSC Ensembl
Innerchr4:67380601..67392963hg19UCSC Ensembl
Outerchr4:67378088..67396101hg19UCSC Ensembl
Innerchr4:67063196..67075558hg18UCSC Ensembl
Outerchr4:67060683..67078696hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3818014
hg1918014
hg1818014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250229, nssv14242646, nssv14241584, nssv14242579
SamplesNGO_41, NGO_24, NGO_47, NGO_40
Known GenesMIR548AJ2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169996
Frequency
Sample Size93
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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