A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891562



Internal ID19185958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10240428..10430602hg38UCSC Ensembl
Outerchr9:10240428..10433023hg38UCSC Ensembl
Innerchr9:10240428..10430602hg19UCSC Ensembl
Outerchr9:10240428..10433023hg19UCSC Ensembl
Innerchr9:10230428..10420602hg18UCSC Ensembl
Outerchr9:10230428..10423023hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38192596
hg19192596
hg18192596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783798, essv25785312
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891562
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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