A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743987



Internal ID18718233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104638750..104638981hg38UCSC Ensembl
Outerchr9:104638652..104639048hg38UCSC Ensembl
Innerchr9:107401031..107401262hg19UCSC Ensembl
Outerchr9:107400933..107401329hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743987
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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