A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001926



Internal ID7067044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:68985630..68996333hg38UCSC Ensembl
Outerchr5:68281457..68292160hg19UCSC Ensembl
Outerchr5:68317213..68327916hg18UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3810704
hg1910704
hg1810704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564231
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001926
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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