A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7736170



Internal ID14811584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134190918..134190919hg38UCSC Ensembl
Outerchr7:134190784..134191054hg38UCSC Ensembl
Innerchr7:133875670..133875671hg19UCSC Ensembl
Outerchr7:133875536..133875806hg19UCSC Ensembl
Innerchr7:133526211..133526210hg18UCSC Ensembl
Outerchr7:133526076..133526346hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38271
hg19271
hg18271
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302805
Supporting Variants
SamplesNA19093
Known GenesLRGUK
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7736170
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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