A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3948042



Internal ID11813830
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1136125
Supporting Variants
SamplesHuRef
Known GenesUGCG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3948042
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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