A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565091



Internal ID6689787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3169172..3176650hg38UCSC Ensembl
Outerchr19:3169170..3176648hg19UCSC Ensembl
Outerchr19:3120170..3127648hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387479
hg197479
hg187479
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005890
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565091
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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