A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564261



Internal ID6688957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:101629589..101641472hg38UCSC Ensembl
Outerchr3:101348433..101360316hg19UCSC Ensembl
Outerchr3:102831123..102843006hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3811884
hg1911884
hg1811884
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992869
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564261
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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