A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7547284



Internal ID10825566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101415921..101417030hg38UCSC Ensembl
Outerchr7:101059202..101060311hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3277717
Supporting Variants
SamplesHuRef
Known GenesCOL26A1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7547284
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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