A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989672



Internal ID7076257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18993945..18993945hg38UCSC Ensembl
chr3:19035437..19035437hg19UCSC Ensembl
chr3:19010441..19010441hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38318
hg19318
hg18318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3566668
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989672
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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