A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7137802



Internal ID10416084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70227894..70237894hg38UCSC Ensembl
Innerchr11:70074000..70084000hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2868235
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7137802
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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