A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7102247



Internal ID10380529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62099509..62139191hg38UCSC Ensembl
Innerchr9:40188000..40228000hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3839683
hg1940001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2832680
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7102247
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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