A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590602



Internal ID16031325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71725034..71754577hg38UCSC Ensembl
Innerchr3:71774185..71803728hg19UCSC Ensembl
Innerchr3:71856875..71886418hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3829544
hg1929544
hg1829544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8373n54
Supporting Variantsnssv965544
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590602
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