A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000067



Internal ID7065202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78999260..79007835hg38UCSC Ensembl
Outerchr15:79291602..79300177hg19UCSC Ensembl
Outerchr15:77078657..77087232hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388576
hg198576
hg188576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563971
SamplesHuRef
Known GenesRASGRF1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000067
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