A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743956



Internal ID18718202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101543271..101543491hg38UCSC Ensembl
Outerchr9:101543255..101543511hg38UCSC Ensembl
Innerchr9:104305553..104305773hg19UCSC Ensembl
Outerchr9:104305537..104305793hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545209
Supporting Variants
Samples
Known GenesRNF20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743956
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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