A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892713



Internal ID19183533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75552756..75578996hg38UCSC Ensembl
Outerchr15:75552756..75578996hg38UCSC Ensembl
Innerchr15:75845097..75871337hg19UCSC Ensembl
Outerchr15:75845097..75871337hg19UCSC Ensembl
Innerchr15:73632152..73658392hg18UCSC Ensembl
Outerchr15:73632152..73658392hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3826241
hg1926241
hg1826241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798239
Samples
Known GenesPTPN9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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