A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564019



Internal ID7035119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29896811..29902447hg38UCSC Ensembl
Outerchr19:30387718..30393354hg19UCSC Ensembl
Outerchr19:35079558..35085194hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg385637
hg195637
hg185637
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992348
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564019
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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