A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1136125



Internal ID11952562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111911906..111911963hg38UCSC Ensembl
chr9:114674186..114674243hg19UCSC Ensembl
chr9:113714007..113714064hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3948042
SamplesHuRef
Known GenesUGCG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1136125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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