A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565096



Internal ID6689792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3735559..3738806hg38UCSC Ensembl
Outerchr1:3652123..3655370hg19UCSC Ensembl
Outerchr1:3641983..3645230hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg383248
hg193248
hg183248
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994567
Supporting Variants
SamplesHuRef
Known GenesTP73, TP73-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565096
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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