A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565055



Internal ID7036155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:96955245..96964359hg38UCSC Ensembl
Outerchr14:97421582..97430696hg19UCSC Ensembl
Outerchr14:96491335..96500449hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389115
hg199115
hg189115
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988078
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565055
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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