A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798239



Internal ID19177852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75552756..75578996hg38UCSC Ensembl
Innerchr15:75845097..75871337hg19UCSC Ensembl
Innerchr15:73632152..73658392hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3826241
hg1926241
hg1826241
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892713
Supporting Variants
Samples
Known GenesPTPN9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798239
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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