A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010299



Internal ID7074364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76303620..76303744hg38UCSC Ensembl
chr8:77215855..77215979hg19UCSC Ensembl
chr8:77378410..77378534hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38125
hg19125
hg18125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3582951
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010299
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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