A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990818



Internal ID7076949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:20968015..20978181hg38UCSC Ensembl
Outerchr5:20968124..20978290hg19UCSC Ensembl
Outerchr5:21003881..21014047hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3810167
hg1910167
hg1810167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564298
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990818
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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