A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564786



Internal ID7035886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:12967308..12981073hg38UCSC Ensembl
Outerchr3:13008808..13022573hg19UCSC Ensembl
Outerchr3:12983808..12997573hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3813766
hg1913766
hg1813766
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999756
Supporting Variants
SamplesHuRef
Known GenesIQSEC1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564786
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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