A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783798



Internal ID19161617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10240428..10430602hg38UCSC Ensembl
Innerchr9:10240428..10430602hg19UCSC Ensembl
Innerchr9:10230428..10420602hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38190175
hg19190175
hg18190175
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891562
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=79
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783798
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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