A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003872



Internal ID7068977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68131847..68137855hg38UCSC Ensembl
Outerchr15:68424185..68430193hg19UCSC Ensembl
Outerchr15:66211239..66217247hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386009
hg196009
hg186009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563951
SamplesHuRef
Known GenesPIAS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003872
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