A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566913



Internal ID7038295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34528011..34528343hg38UCSC Ensembl
chr20:33115816..33116148hg19UCSC Ensembl
chr20:32579477..32579809hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38333
hg19333
hg18333
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002762
Supporting Variants
SamplesHuRef
Known GenesDYNLRB1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566913
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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