A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161428



Internal ID7906142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9647540..9887820hg38UCSC Ensembl
Innerchr9:9647540..9887820hg19UCSC Ensembl
Innerchr9:9637540..9877820hg18UCSC Ensembl
Innerchr9:9637540..9877820hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38240281
hg19240281
hg18240281
hg17240281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422381
Supporting Variants
SamplesND04152
Known GenesPTPRD
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161428
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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