A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544881



Internal ID18399271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69189635..69190022hg38UCSC Ensembl
Outerchr9:69189538..69190118hg38UCSC Ensembl
Innerchr9:71804551..71804938hg19UCSC Ensembl
Outerchr9:71804454..71805034hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743628
Samples
Known GenesTJP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544881
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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