A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006029



Internal ID18748560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73928205..74120947hg38UCSC Ensembl
Innerchr4:74793922..74986664hg19UCSC Ensembl
Innerchr4:75012786..75205528hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38192743
hg19192743
hg18192743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633821
Samples
Known GenesCXCL2, CXCL3, CXCL5, PF4, PPBP, PPBPP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006029
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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