A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7112247



Internal ID10390529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67439979..67489501hg38UCSC Ensembl
Innerchr9:65808000..65858000hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3849523
hg1950001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2842680
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7112247
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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