A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565430



Internal ID7036812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114076721..114085606hg38UCSC Ensembl
Outerchr9:116839001..116847886hg19UCSC Ensembl
Outerchr9:115878822..115887707hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg388886
hg198886
hg188886
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996359
Supporting Variants
SamplesHuRef
Known GenesAMBP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565430
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