A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565300



Internal ID6689996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13322792..13328754hg38UCSC Ensembl
Outerchr10:13364792..13370754hg19UCSC Ensembl
Outerchr10:13404798..13410760hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385963
hg195963
hg185963
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010238
Supporting Variants
SamplesHuRef
Known GenesSEPHS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565300
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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