A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797423



Internal ID19180606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8922286..8940141hg38UCSC Ensembl
Innerchr9:8922286..8940141hg19UCSC Ensembl
Innerchr9:8912286..8930141hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3817856
hg1917856
hg1817856
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891555
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797423
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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