A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7123359



Internal ID10054955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1028634..1029122hg38UCSC Ensembl
Outerchr1:964014..964502hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2853792
Supporting Variants
SamplesHuRef
Known GenesAGRN
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7123359
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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