A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3926893



Internal ID11834979
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1132189
Supporting Variants
SamplesHuRef
Known GenesSETX
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3926893
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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