A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5477490



Internal ID9232468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20573474..20575620hg38UCSC Ensembl
Outerchr7:20573437..20575670hg38UCSC Ensembl
Innerchr7:20613097..20615243hg19UCSC Ensembl
Outerchr7:20613060..20615293hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676078
Supporting Variants
SamplesNA11920
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5477490
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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