A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1132189



Internal ID12295312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132270122..132270204hg38UCSC Ensembl
chr9:135145509..135145591hg19UCSC Ensembl
chr9:134135330..134135412hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3926893
SamplesHuRef
Known GenesSETX
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1132189
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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