A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006379



Internal ID6718498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35307669..35319918hg38UCSC Ensembl
Outerchr19:35798572..35810821hg19UCSC Ensembl
Outerchr19:40490412..40502661hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812250
hg1912250
hg1812250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565539
SamplesHuRef
Known GenesMAG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006379
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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