A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006678



Internal ID7071771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149979956..149986405hg38UCSC Ensembl
Outerchr4:150901108..150907557hg19UCSC Ensembl
Outerchr4:151120558..151127007hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg386450
hg196450
hg186450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563925
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006678
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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