A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565233



Internal ID6689929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10176180..10183265hg38UCSC Ensembl
Outerchr19:10286856..10293941hg19UCSC Ensembl
Outerchr19:10147856..10154941hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387086
hg197086
hg187086
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001261
Supporting Variants
SamplesHuRef
Known GenesDNMT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565233
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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