A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744012



Internal ID18371572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106913633..106914180hg38UCSC Ensembl
Outerchr9:106913619..106914295hg38UCSC Ensembl
Innerchr9:109675914..109676461hg19UCSC Ensembl
Outerchr9:109675900..109676576hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545265
Supporting Variants
Samples
Known GenesMIR548Q, ZNF462
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744012
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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