A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545558



Internal ID18746634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132883699..132884673hg38UCSC Ensembl
Outerchr9:132883444..132884744hg38UCSC Ensembl
Innerchr9:135759086..135760060hg19UCSC Ensembl
Outerchr9:135758831..135760131hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744305
Samples
Known GenesC9orf9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545558
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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