A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988366



Internal ID7075637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:30896881..30901709hg38UCSC Ensembl
Outerchr8:30754397..30759225hg19UCSC Ensembl
Outerchr8:30873939..30878767hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382413
hg192413
hg182413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564232
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988366
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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