A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563566



Internal ID7036326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32416550..32417155hg38UCSC Ensembl
Outerchr10:32705478..32706083hg19UCSC Ensembl
Outerchr10:32745484..32746089hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996545
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563566
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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