A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250416



Internal ID21310658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37504706..37514035hg38UCSC Ensembl
Outerchr9:37502112..37515714hg38UCSC Ensembl
Innerchr9:37504703..37514032hg19UCSC Ensembl
Outerchr9:37502109..37515711hg19UCSC Ensembl
Innerchr9:37494703..37504032hg18UCSC Ensembl
Outerchr9:37492109..37505711hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813603
hg1913603
hg1813603
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169673
Supporting Variants
SamplesNGO_9
Known GenesFBXO10, POLR1E
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250416
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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