A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564481



Internal ID6689177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9474447..9476740hg38UCSC Ensembl
Outerchr19:9585123..9587416hg19UCSC Ensembl
Outerchr19:9446123..9448416hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382294
hg192294
hg182294
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995010
Supporting Variants
SamplesHuRef
Known GenesZNF560
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564481
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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