A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011195



Internal ID6723283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:39289377..39293024hg38UCSC Ensembl
Outerchr3:39330868..39334515hg19UCSC Ensembl
Outerchr3:39305872..39309519hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383512
hg193512
hg183512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564322
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011195
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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