A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161480



Internal ID7906194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11512989..11675590hg38UCSC Ensembl
Innerchr9:11512989..11675590hg19UCSC Ensembl
Innerchr9:11502989..11665590hg18UCSC Ensembl
Innerchr9:11502989..11665590hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38162602
hg19162602
hg18162602
hg17162602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422486
Supporting Variants
SamplesND01701
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161480
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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