A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545358



Internal ID18746434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115095468..115095658hg38UCSC Ensembl
Outerchr9:115095431..115095702hg38UCSC Ensembl
Innerchr9:117857747..117857937hg19UCSC Ensembl
Outerchr9:117857710..117857981hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744105
Samples
Known GenesTNC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545358
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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