A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5523688



Internal ID8501091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:224466..225772hg38UCSC Ensembl
Outerchr7:224095..226142hg38UCSC Ensembl
Innerchr7:224466..225772hg19UCSC Ensembl
Outerchr7:224095..226142hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2656552
Supporting Variants
SamplesNA19373
Known GenesFAM20C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5523688
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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