A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004657



Internal ID7069753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83416037..83422010hg38UCSC Ensembl
Outerchr15:84084789..84090762hg19UCSC Ensembl
Outerchr15:81875793..81881766hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384166
hg194166
hg184166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565709
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004657
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