A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996110



Internal ID7080420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129490858..129499186hg38UCSC Ensembl
Outerchr9:132253137..132261465hg19UCSC Ensembl
Outerchr9:131292958..131301286hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388329
hg198329
hg188329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564219
SamplesHuRef
Known GenesLINC00963
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996110
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