A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751293



Internal ID18725539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62413933..62415554hg38UCSC Ensembl
Outerchr15:62413794..62415662hg38UCSC Ensembl
Innerchr15:62706132..62707753hg19UCSC Ensembl
Outerchr15:62705993..62707861hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751293
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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