A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545291



Internal ID18746367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109667979..109668232hg38UCSC Ensembl
Outerchr9:109667913..109668290hg38UCSC Ensembl
Innerchr9:112430259..112430512hg19UCSC Ensembl
Outerchr9:112430193..112430570hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744038
Samples
Known GenesPALM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545291
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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