A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552212



Internal ID18753288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24870562..24872356hg38UCSC Ensembl
Outerchr15:24870534..24872606hg38UCSC Ensembl
Innerchr15:25115709..25117503hg19UCSC Ensembl
Outerchr15:25115681..25117753hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382073
hg192073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750959
Samples
Known GenesSNRPN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552212
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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