A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894094



Internal ID19184948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188339654..188741515hg38UCSC Ensembl
Outerchr4:188223645..189006348hg38UCSC Ensembl
Innerchr4:189260808..189662669hg19UCSC Ensembl
Outerchr4:189144799..189927502hg19UCSC Ensembl
Innerchr4:189497802..189899663hg18UCSC Ensembl
Outerchr4:189381793..190164496hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38782704
hg19782704
hg18782704
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784623, essv25781237, essv25789371
Samples
Known GenesLINC01060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894094
Frequency
Sample Size3017
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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