A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008907



Internal ID7058953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10414447..10414447hg38UCSC Ensembl
chr18:10414444..10414444hg19UCSC Ensembl
chr18:10404444..10404444hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3569677
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008907
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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