A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1401355



Internal ID12564478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107361582..107361672hg38UCSC Ensembl
chr8:108373810..108373900hg19UCSC Ensembl
chr8:108442986..108443076hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3891
hg1991
hg1891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3639978
SamplesHuRef
Known GenesANGPT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1401355
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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