A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563513



Internal ID6688868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3772970..3783841hg38UCSC Ensembl
Outerchr19:3772968..3783839hg19UCSC Ensembl
Outerchr19:3723968..3734839hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810872
hg1910872
hg1810872
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011184
Supporting Variants
SamplesHuRef
Known GenesMATK
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563513
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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