A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552612



Internal ID18407002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68421002..68421183hg38UCSC Ensembl
Outerchr15:68420960..68421229hg38UCSC Ensembl
Innerchr15:68713341..68713522hg19UCSC Ensembl
Outerchr15:68713299..68713568hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751359
Samples
Known GenesITGA11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552612
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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