A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552696



Internal ID18753772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76044394..76054092hg38UCSC Ensembl
Outerchr15:76043660..76054418hg38UCSC Ensembl
Innerchr15:76336735..76346433hg19UCSC Ensembl
Outerchr15:76336001..76346759hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3810759
hg1910759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751443
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552696
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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