A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891564



Internal ID18839274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9553037..11021845hg38UCSC Ensembl
Outerchr9:9553037..11021845hg38UCSC Ensembl
Innerchr9:9553037..11021845hg19UCSC Ensembl
Outerchr9:9553037..11021845hg19UCSC Ensembl
Innerchr9:9543037..11011845hg18UCSC Ensembl
Outerchr9:9543037..11011845hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381468809
hg191468809
hg181468809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792515
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891564
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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