A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7106691



Internal ID10384973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61198806..61208775hg38UCSC Ensembl
Innerchr9:43612000..43622000hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389970
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2837124
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7106691
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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