A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594943



Internal ID16035666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98893976..98895600hg38UCSC Ensembl
Innerchr4:99815127..99816751hg19UCSC Ensembl
Innerchr4:100034150..100035774hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381625
hg191625
hg181625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1003438
Samples
Known GenesEIF4E
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594943
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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