A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741877



Internal ID18369437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16089433..16165726hg38UCSC Ensembl
Outerchr8:16087492..16166491hg38UCSC Ensembl
Innerchr8:15946942..16023235hg19UCSC Ensembl
Outerchr8:15945001..16024000hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3879000
hg1979000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543130
Supporting Variants
Samples
Known GenesMSR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741877
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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