A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739748



Internal ID18713994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:828269..831505hg38UCSC Ensembl
Outerchr7:827709..831567hg38UCSC Ensembl
Innerchr7:867906..871142hg19UCSC Ensembl
Outerchr7:867346..871204hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541001
Supporting Variants
Samples
Known GenesSUN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739748
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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