A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892734



Internal ID18836868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96765358..96861598hg38UCSC Ensembl
Outerchr15:96765358..96861598hg38UCSC Ensembl
Innerchr15:97308588..97404828hg19UCSC Ensembl
Outerchr15:97308588..97404828hg19UCSC Ensembl
Innerchr15:95109592..95205832hg18UCSC Ensembl
Outerchr15:95109592..95205832hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3896241
hg1996241
hg1896241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799684
Samples
Known GenesSPATA8, SPATA8-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892734
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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