A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744183



Internal ID18718429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123913722..123918995hg38UCSC Ensembl
Outerchr9:123913222..123920221hg38UCSC Ensembl
Innerchr9:126676001..126681274hg19UCSC Ensembl
Outerchr9:126675501..126682500hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545436
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744183
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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