A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563992



Internal ID7035092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:80095206..80109418hg38UCSC Ensembl
Outerchr13:80669341..80683553hg19UCSC Ensembl
Outerchr13:79567342..79581554hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3814213
hg1914213
hg1814213
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001493
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563992
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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