A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002892



Internal ID7068004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32982558..32982691hg38UCSC Ensembl
chr20:31570364..31570497hg19UCSC Ensembl
chr20:31034025..31034158hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38134
hg19134
hg18134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574780
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002892
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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