A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565642



Internal ID7037024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:57392203..57402960hg38UCSC Ensembl
Outerchr5:56688030..56698787hg19UCSC Ensembl
Outerchr5:56723787..56734544hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810758
hg1910758
hg1810758
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994015
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565642
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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