A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595447



Internal ID16382856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132239582..132330899hg38UCSC Ensembl
Innerchr4:133160737..133252054hg19UCSC Ensembl
Innerchr4:133380187..133471504hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3891318
hg1991318
hg1891318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1006515
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595447
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