A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564866



Internal ID7035966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1684981..1692324hg38UCSC Ensembl
Outerchr19:1684980..1692323hg19UCSC Ensembl
Outerchr19:1635980..1643323hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387344
hg197344
hg187344
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990088
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564866
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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