A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788011



Internal ID18831116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9729134..10077180hg38UCSC Ensembl
Innerchr9:9729134..10077180hg19UCSC Ensembl
Innerchr9:9719134..10067180hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38348047
hg19348047
hg18348047
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891565
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=120
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788011
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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