A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751346



Internal ID18725592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67576063..67576917hg38UCSC Ensembl
Outerchr15:67575957..67577138hg38UCSC Ensembl
Innerchr15:67868401..67869255hg19UCSC Ensembl
Outerchr15:67868295..67869476hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552599
Supporting Variants
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751346
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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