A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565707



Internal ID6690403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11575212..11587674hg38UCSC Ensembl
Outerchr19:11686027..11698489hg19UCSC Ensembl
Outerchr19:11547027..11559489hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812463
hg1912463
hg1812463
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991647
Supporting Variants
SamplesHuRef
Known GenesACP5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565707
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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