A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2853792



Internal ID10526772
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 StatusM
Merged Variants
Supporting Variantsessv7123359
SamplesHuRef
Known GenesAGRN
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2853792
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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