A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1312882



Internal ID12476004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22708974..22709390hg38UCSC Ensembl
chr8:22566487..22566903hg19UCSC Ensembl
chr8:22622432..22622848hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38417
hg19417
hg18417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3939316
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1312882
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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