A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1764616



Internal ID5894716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23040301..23040377hg38UCSC Ensembl
chr8:22897814..22897890hg19UCSC Ensembl
chr8:22953759..22953835hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3877
hg1977
hg1877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4135499
SamplesHuRef
Known GenesTNFRSF10B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1764616
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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