A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997089



Internal ID6733031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:43630014..43641441hg38UCSC Ensembl
Outerchr7:43669613..43681040hg19UCSC Ensembl
Outerchr7:43636138..43647565hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3811428
hg1911428
hg1811428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565020
SamplesHuRef
Known GenesCOA1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997089
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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