A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005890



Internal ID6718011
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565091
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005890
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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