A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565819



Internal ID7037201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:151045540..151045895hg38UCSC Ensembl
Outerchr2:151902054..151902409hg19UCSC Ensembl
Outerchr2:151610300..151610655hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38356
hg19356
hg18356
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998123
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565819
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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