A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010667



Internal ID7074618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:14832964..14837552hg38UCSC Ensembl
Outerchr4:14834588..14839176hg19UCSC Ensembl
Outerchr4:14443686..14448274hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg384188
hg194188
hg184188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563459
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010667
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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