A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7118580



Internal ID10050176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:168055331..168056504hg38UCSC Ensembl
Outerchr1:168024569..168025742hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2849013
Supporting Variants
SamplesHuRef
Known GenesDCAF6
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7118580
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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