A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7113358



Internal ID10391640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67513501..67519501hg38UCSC Ensembl
Innerchr9:65882000..65888000hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2843791
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7113358
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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