A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743928



Internal ID18371488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98238053..98238826hg38UCSC Ensembl
Outerchr9:98237869..98238937hg38UCSC Ensembl
Innerchr9:101000335..101001108hg19UCSC Ensembl
Outerchr9:101000151..101001219hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545181
Supporting Variants
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743928
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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