A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792515



Internal ID18815246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9553037..11021845hg38UCSC Ensembl
Innerchr9:9553037..11021845hg19UCSC Ensembl
Innerchr9:9543037..11011845hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381468809
hg191468809
hg181468809
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891564
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=498
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792515
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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