A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009766



Internal ID6721865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:8066482..8094656hg38UCSC Ensembl
Outerchr7:8106112..8134286hg19UCSC Ensembl
Outerchr7:8072637..8100811hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3828175
hg1928175
hg1828175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563501
SamplesHuRef
Known GenesGLCCI1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009766
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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