A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744147



Internal ID18371707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203817385..203818325hg38UCSC Ensembl
Outerchr1:203817338..203818435hg38UCSC Ensembl
Innerchr1:203786513..203787453hg19UCSC Ensembl
Outerchr1:203786466..203787563hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545400
Supporting Variants
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744147
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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