A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751363



Internal ID18725609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68691342..68691611hg38UCSC Ensembl
Outerchr15:68691313..68691636hg38UCSC Ensembl
Innerchr15:68983681..68983950hg19UCSC Ensembl
Outerchr15:68983652..68983975hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552616
Supporting Variants
Samples
Known GenesCORO2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751363
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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